Targeted gene expression profiling for accurate endometrial receptivity testing

Expressional profiling of the endometrium enables the personalised timing of the window of implantation (WOI). This study presents and evaluates a novel analytical pipeline based on a TAC-seq (Targeted Allele Counting by sequencing) method for endometrial dating. The expressional profiles were clustered, and differential expression analysis was performed on the model development group, using 63 endometrial biopsies spanning over proliferative (PE, n = 18), early-secretory (ESE, n = 18), mid-secretory (MSE, n = 17) and late-secretory (LSE, n = 10) endometrial phases of the natural cycle. A quantitative predictor model was trained on the development group and validated on sequenced samples from healthy women, consisting of 52 paired samples taken from ESE and MSE phases and five LSE phase samples from 31 individuals. Finally, the developed test was applied to 44 MSE phase samples from a study group of patients diagnosed with recurrent implantation failure (RIF). In validation samples (n = 57), we detected displaced WOI in 1.8% of the samples from fertile women. In the RIF study group, we detected a significantly higher proportion of the samples with shifted WOI than in the validation set of samples from fertile women, 15.9% and 1.8% (p = 0.012), respectively. The developed model was evaluated with an average cross-validation accuracy of 98.8% and an accuracy of 98.2% in the validation group. The developed beREADY screening model enables sensitive and dynamic detection of selected transcriptome biomarkers, providing a quantitative and accurate prediction of endometrial receptivity status.

endometrium is considered to become receptive seven days after the luteinising hormone (LH) peak during the natural cycle (NC) and lasts for two days.However, several studies suggest that the length of the WOI may vary from two to up to 6 days [3][4][5][6] .In addition, based on transcriptional studies of endometrial biopsies, the WOI can be shifted or displaced over time 7,8 .It has been estimated that displaced WOI occurs in around 10% of women undergoing IVF and at least 25% with RIF 6,[9][10][11] .In this light, the personalised determination of the WOI timing could be a standard procedure for women undergoing IVF.This would be crucial to avoid implantation failure after embryo transfer, possibly due to the asynchrony between the endometrial and embryonal development.Therefore, testing the endometrial receptivity and establishing the time for WOI may be particularly beneficial for RIF patients.
Polycystic ovary syndrome (PCOS) is an infertility-associated disorder common among women of reproductive age.It is still unclear whether endometrial receptivity is affected in PCOS patients.The dysregulation of several endometrial receptivity-associated genes in PCOS patients has been previously described 12 .Besides the altered gene expression profile of endometrial tissue, PCOS patients are often affected by obesity, hyperinsulinemia, and increased general inflammation, likely contributing to infertility 13 .Nevertheless, to our knowledge, no systematic studies have been published describing the gene expression signature of essential endometrial receptivity genes in PCOS throughout the entire menstrual cycle.
Considerable effort has been made to describe molecular changes in the WOI 14,15 .The hormone-induced regulatory cascade leads to endometrial maturation and major gene expression changes, culminating with the opening of the WOI.The transcriptomic landscape of endometrial maturation is well characterised through whole transcriptome studies where different gene expression profiles have been detected between proliferative (PE), early-(ESE), mid-(MSE), and late-secretory (LSE) endometrium 14,16,17 .Based on these studies, biomarkers for WOI determination and personalised embryo transfer (pET) have been provided.Diagnostic tests based on gene expression profiling of varying sets of endometrial receptivity biomarkers have been developed and integrated into infertility treatment [18][19][20][21] .Endometrial receptivity tests currently in clinical use are the ERA ® test (Igenomix) 18 , the ER Map ® test (IGLS) 20 , the WIN-Test (INSERM) 21 , and the rsERT test (Yikon Genomics Company) 10 .Compared to the targeted sequencing approach used in the present study, these tests are limited either by the sensitivity and dynamic range in detecting transcript abundances or by the scalability of the technique applied.
This study introduces the beREADY model for reliable WOI detection.The 72 genes analysed with this test contain 57 endometrial receptivity-associated biomarkers 22 , 11 additional genes relevant to WOI, and four housekeeper genes.The computational model was developed using Illumina sequencing-based TAC-seq technology (Targeted Allele Counting by sequencing), enabling biomolecule analysis down to a single-molecule level 23 , as shown in Fig. 1.

Gene expression profiling of PCOS samples. This analysis of endometrial receptivity biomarkers
revealed no difference between healthy women and PCOS patients (Fig. 2).Comparative t-testing and ANOVA of individual genes did not reveal any significantly (FDR < 0.05) differentially expressed genes between the groups of PCOS patients and healthy women (Suppl.Table 1).These results were observed in all four menstrual cycle phases (Fig. 2) and confirmed by principal component analysis (Suppl.Fig. 2).Based on these results, we concluded that PCOS status does not affect the expression profiles of biomarkers included in the developed assay.beREADY model development.Before test development, 11 samples from the MD group were excluded from downstream analysis due to inconsistency between histology results and LH-day measurements.The remaining 63 MD group samples clustered clearly according to the menstrual cycle phases and enabled determining the receptivity class prediction (Fig. 3).When the PE phase and ESE samples were analysed together, the signature of receptivity genes allowed the discrimination of three groups of pre-receptive (PE and ESE samples), receptive (MSE samples), and post-receptive (LSE) samples (Suppl.Fig. 3).According to predicted menstrual cycle phase probabilities, the MSE endometria (n = 17) were defined as receptive, corresponding to WOI.The PE and ESE endometrial samples (n = 36) were classified as pre-receptive, suggesting that the endometrium has not yet reached the WOI.The LSE endometria (n = 10) were defined as post-receptive, reflecting the period after WOI (Fig. 4).Based on fivefold cross-validation, the predictive model classified PE/ESE, MSE, and LSE samples with 98.8% accuracy, averaged over all the receptivity classes.
Endometrial samples with two similar receptivity classes were classified as belonging to a transitionary class.Samples between the pre-receptive and receptive groups were defined as early-receptive and samples between receptive and post-receptive as late-receptive.However, samples positioned in the early-receptive, receptive, or late-receptive groups were collectively considered to represent the normal variability of WOI.beREADY model validation.Endometrial tissue samples from healthy volunteers (MV group) were used for classification accuracy validation.In total, tissue samples from NC ESE (n = 26), MSE (n = 26), and LSE (n = 5) phases were analysed (Table 1).The test evaluated all ESE samples as pre-receptive.Considering the MSE group, 25 samples were classified as receptive (25/26, 96.2%), from which six samples were classified as earlyreceptive (6/26, 23.1%) (Table 2).One sample from the MSE group (1/26, 3.8%) was classified as pre-receptive, concordant with prior histological evaluation.All LSE validation group samples were classified as post-receptive samples (Fig. 5).In conclusion, all samples with concordant histological and LH dating were classified to the expected receptivity group, while one biopsy (1/57, 1.8%) demonstrated a discrepancy with the beREADY classification.It is relevant to note that a slight WOI shift, within the normal variability of the WOI range, was detected in almost every fourth healthy woman (23.1%) in MSE (Table 2).

RIF group study.
Finally, a group of infertile women with RIF diagnosis (n = 44) were analysed.Out of the RIF MSE samples, three patients (3/44, 6.8%) had a pre-receptive profile and displaced WOI (Table 2).No late-receptive samples were detected, but four displayed a post-receptive profile (4/44, 9.1%).Additionally, eight patients (8/44, 18.2%) were in the normal variability of the WOI range but deviated slightly from the receptive expressional profile and were classified as early-receptive.As a result, displaced WOI was detected in 15.9% of the samples in the RIF group.The proportion of the endometrial samples with the displaced WOI was higher in the RIF group than in the MV group, composed of healthy women, 15.9% and 1.8%, respectively (p = 0.012).

Discussion
This study presents a novel tool for measuring endometrial receptivity.It is based on a highly quantitative TAC-seq assay that allows precise and cost-effective endometrial receptivity biomarker analysis.A custom computational model for classifying sequenced samples was developed to analyse data generated by the TAC-seq pipeline.As it is based on the expressional profile of a targeted set of genes, the beREADY classification model can be used in high-coverage whole-transcriptome studies.As a result, using endometrial biomarkers discovered www.nature.com/scientificreports/from datasets with high predictive power for receptivity 22,24 , our prediction model allows the construction of the continuous transcriptomic states of endometrial receptivity development.
Previous transcriptomic studies of endometrium have shed light on the complex cross-talk mechanism between implanting embryos and the uterus.This insight has explained why embryo implantation in some women repeatedly fails, regardless of the use of seemingly high-quality embryos 3,14,25 .Therefore, the focus on helping RIF patients has shifted towards elucidating the maternal factors contributing to unsuccessful IVF cycles.This interest has propagated the development of transcriptomic analysis tools for determining the receptivity status of the endometrium 10,18,20,21 .Those tests use varying sets of targeted genes and different methodologies.
The ERA test analyses 238 receptivity genes using microarray technology, Map ® /ER Grade ® test, and ERPeakSM test analyses 40 genes and WIN-Test 11 genes with quantitative PCR.The selection of genes in the beREADY model is based on the comprehensive meta-analysis of endometrial receptivity biomarkers 22 , complemented by eleven additional genes relevant for WOI and four housekeeper genes.To our knowledge, the beREADY model is the only endometrial receptivity testing tool that applies the Unique Molecular Identifiers (UMI) technology, enabling original transcript counts estimation while avoiding the PCR-caused bias in results.Therefore, TACseq technology eliminates laboratory-caused PCR duplicates and counts the biomarkers at a single-molecule level 23 .This approach has already been used to determine the menstrual cycle phases from endometrial tissue 26 .
For beREADY model development, we used natural cycle endometrial samples from healthy women and women with PCOS diagnosis.Although the involvement of endometrial factors in PCOS-associated infertility has been suggested (reviewed in Piltonen, 2016) 13 , there are no large-scale and systematic studies simultaneously analysing numerous endometrial receptivity-related genes in different cycle phases in PCOS patients.In addition, the endometrial tissues of PCOS patients have demonstrated altered responses to steroids 27,28 , but the overall effect of endometrial dysfunction on pregnancy outcomes is still unclear 29 .Therefore, we tested if PCOS alters the transcriptomic profiles of our selection of receptivity biomarkers.We found no significant differences between healthy controls and PCOS patients in the expression profile of endometrial biomarkers throughout the menstrual cycle from PE to the LSE phase.Based on these findings, we concluded that the selected receptivity biomarkers are unaffected in women with PCOS, and the samples were suitable for use as a reference together with samples from healthy women in the development of the beREADY model.One of the contributing factors to why we did not see significant differences in the expressional profiles of PCOS and healthy samples is that some women in the test development group had lost their PCOS characteristics since their initial diagnosis due to ageing.Nevertheless, it must be noted that PCOS is a lifelong condition despite the effect of ageing and that a retrospective diagnosis is allowed 30 .Secondly, patients in our study were not obese.When combined, PCOS and obesity can still introduce an additional risk factor for impaired endometrial receptivity 31 .For these reasons, our conclusions regarding receptivity in PCOS patients are valid for women with PCOS patients within the normal range of BMI.
We validated the beREADY model by analysing endometrial biopsies from healthy women representing the fertile female population, displaying a high similarity between sample collection time and the molecular test result (56/57, 98.2%).This similarity can be explained by the fact that the healthy women in our validation group were all LH tested and had ultrasound confirmation of ovulation and normal hormonal values.Despite this, one MSE sample (1/26, 3.8%) with corresponding tissue morphology suggested the PE phase had shifted WOI according to the beREADY.In that case, the beREADY model classified the sample as pre-receptive, suggesting www.nature.com/scientificreports/ that the WOI had not yet arrived.However, displaced WOI among oocyte donors and women undergoing IVF without RIF diagnosis has been previously reported 11,32 .In the MSE group, we also classified six samples as earlyreceptive (6/26, 23.1%), suggesting a slight shift in WOI that remained within the normal range of receptivity.Therefore, transcriptomic profiling can offer additional accuracy for determining the individual receptivity timing of the endometrium.The criteria for RIF diagnosis are controversial and include several factors, such as the number of failed treatment cycles, the number of transferred good-quality embryos and maternal age 33 .Due to its heterogeneous nature, the causes of RIF have remained largely unknown.When focusing solely on endometrial factors, it has been proposed by Sebastian-Leon et al. that RIF is caused by at least two distinct molecular phenomena of displaced (asynchronous) or disrupted (pathological) WOI 8 .In our study, we applied the beREADY model to detect the rate of displaced WOI in a study group of 44 RIF patients.In total, we detected shifted WOI in 15.9% of RIF cases, which is slightly less than the results described previously by Lessey et   25 in women with RIF diagnosis.Compared with the MV group, the RIF study group demonstrated a significantly higher proportion of shifted WOI cases (p < 0.05), indicating that displaced WOI can cause RIF.Moreover, Eisman et al. described a significant decrease in ongoing pregnancy rates in the RIF cohort with asynchronous endometrium compared to control infertile patients with detected WOI displacement 35 , suggesting that there are additional factors in implantation failure beyond an adjustment in progesterone exposure.Indeed, in RIF cases, additional endometrial-related factors likely contribute to the implantation failure along the displaced or disrupted WOI, like dysbiotic vaginal or uterine microbiome 36,37 .
Evidence on the clinical effectiveness of endometrial receptivity testing on the IVF pregnancy rate is still controversial.Several studies have demonstrated a significant increase in implantation rate with pET with ERA 19,38 , Win-test 3 and rsERT 10 tests.It has also been proposed that receptivity testing before the first embryo transfer increases the implantation and cumulative pregnancy rates when pET is compared with conventional embryo transfers 19 .Contrary to those reports, recent randomised controlled trials (RCT) and meta-analyses question the effectiveness of endometrial testing and find its impact insignificant [39][40][41][42] .Although other similar systematic meta-analyses and single cohort studies confirm these results of no benefit of WOI testing in good prognosis patients, they also report that in the RIF subgroup, there is a significant increase in pregnancy rates following pET 38,43,44 .Another study by Haouzi et al. demonstrated that the implantation rate increased over three times, from 7 to 23%, after using the personalised WOI determination in IVF patients with RIF diagnosis 3 .Despite generally supporting endometrial testing in RIF cases, these studies also stress low certainty of evidence, thus advocating continued research on this controversial topic 38,43,44 .One reason for the disparity between studies might be that the actual rate of recurrent implantation failure due to endometrial factors may be lower than previously thought.A large-scale retrospective study involving nearly 4500 patients undergoing IVF with preimplantation genetic testing for aneuploidy (PGT-A) discovered that only around 5% of the infertile patients failed to achieve clinical pregnancy following three consecutive frozen euploid single embryo transfers 45 .Embryonic and maternal factors such as embryonal chromosomal aberrations, impaired endometrial receptivity, maternal immune dysfunction, and infertility-associated diseases, like endometriosis and male factors, can all affect the chance of embryo implantation.Therefore, due to the challenges related to the high heterogeneity of the study designs and groups, only specific subgroups of women might benefit from the endometrial receptivity testing.In summary, personalised endometrial dating likely increases the chance of implantation in patients with recurrent IVF failure.At the same time, it is considered an unnecessary 'add-on' for patients planning their first IVF treatment.However, the overall efficacy of the approach is still largely unclear due to the disparity between the large-scale studies and the transcriptomic tests applied.
The potential clinical utility of endometrial receptivity testing is also fully dependent upon the consistency of the gene expression profile in subsequent cycles following the endometrial biopsy.Indeed, this claim has been approved by the seminal paper of Díaz-Gimeno et al. 46 .In this study, the authors demonstrated the reproducibility of the endometrial receptivity testing, as seven women underwent ERA testing twice.The second endometrial biopsy was obtained from these women on the same day of their menstrual cycle between 29 and 40 months after the first study cycle.The intercycle variation analysis showed total consistency in the ERA test diagnoses between the same patient's first and second tests.Therefore, it is believed that the gene expression profile of the endometrial receptivity remains consistent in time, at least for the subsequent couple of months after biopsy, allowing the embryo transfer time to be adjusted according to the endometrial receptivity test recommendations.This personalised embryo transfer would allow to select the time period with the peak of endometrial receptivity for embryo transfer.However, as the initial study involved only seven patients, the question about the endometrial profile's cycle-to-cycle consistency requires further studies.
Moreover, using the endometrial tissue biopsy for its receptivity testing would exclude the possibility of embryo transfer in the same cycle, thereby prolonging IVF treatment.Considering the possible cycle-to-cycle variation of the window of implantation timing, the endometrial receptivity testing could benefit if it could be analysed non-invasively at the cycle when embryos are planned to be transferred.Receptivity assessment from uterine fluid would circumvent the abovementioned problems, as uterine fluid aspiration can be done before embryo transfer, which is not detrimental to the implantation rate 47,48 .Recently, we provided proof for RNA biomarker-based minimally invasive endometrial receptivity testing using uterine fluid-derived extracellular vesicles and applying the beREADY endometrial testing model to successfully determine the receptivity status of the samples 49 .A similar approach would open new possibilities for non-invasive endometrial receptivity testing, which may eliminate the main shortcomings of the endometrial biopsy-based approaches in personalised embryo transfer.
Some limitations of this study should also be noted.Although the MD set consisted of samples with clearly different expressional profiles corresponding to the different menstrual cycle phases, this study suffers from a relatively small sample size with uneven distribution of samples between the receptivity classes.Furthermore, www.nature.com/scientificreports/ to estimate the clinical usefulness of the model, an extensive RCT must be carried out among the RIF patients, comparing the implantation, pregnancy, and live birth rates between pET and conventional embryo transfer cycles.Ideally, the RCT should be carried out with euploid embryos following PGT-A, which could rule out the genetic defects of IVF embryos as one of the possible causes of implantation failure.PGT-A has been shown to improve the cumulative IVF pregnancy outcome, avoiding the RIF diagnosis in some patients because of the transfer of the euploid embryos only 45 .Therefore, in our study, the RIF samples with possibly embryo-associated implantation failure were not excluded, likely explaining why in our findings the receptive endometrium was found in around 85% of RIF cases.
In conclusion, our results demonstrate that TAC-seq can be successfully applied for transcriptomic endometrial dating and establishing of the WOI.This assay detected distinct profiles of endometrial samples at prereceptive, receptive, and post-receptive stages.Additionally, we found no significant difference in the expression levels of receptivity biomarkers in healthy fertile women and women diagnosed with PCOS.Based on these findings, we developed the beREADY endometrial receptivity testing tool with a custom classification model for distinguishing between the transcriptional profiles.In our study, we detected an increased rate of displaced WOI cases in the RIF study group compared to the validation group.Consequently, these findings suggest that applying personalised receptivity testing before embryo transfer could potentially reduce the chance of implantation failure in RIF patients.

Materials and methods
All methods were carried out in accordance with relevant guidelines and regulations' or the 'Declaration of Helsinki' .
Patient selection and sample collection.Three different study groups were used for the training and testing of the beREADY model.The general characteristics of these groups are presented in Table 1.The menstrual cycle phase was confirmed by menstrual cycle history and LH peak measurement using Clearblue ® digital ovulation test or BabyTime hLH urine cassette (Pharmanova).Endometrial histological evaluation of biopsies was done according to Noyes' criteria.None of the women had been using hormonal medications for at least three months before the biopsy.All endometrial tissue biopsies were collected using a Pipelle ® flexible suction catheter (Laboratoire CCD, France).
Model training and development group.Endometrial samples in the MD group were collected from different menstrual cycle phases of the NC from healthy fertile volunteers (n = 35) and women with PCOS (n = 39) at the Oulu University Hospital (Finland), Table 1.The healthy BMI-matched controls for the PCOS group had a regular menstrual cycle without any signs of PCOS or endometriosis.The women with PCOS were identified from the hospital register based on their prior diagnosis of PCOS (Rotterdam criteria).Their current PCOS phenotype was confirmed by interview, clinical examination, and vaginal ultrasonographic examination of ovaries (Voluson 730 Expert).All women with PCOS diagnosis had ongoing or previous polycystic ovarian morphology, current or previous oligomenorrhea, and two had signs of clinical hyperandrogenism.In healthy and PCOS groups, PE, ESE, MSE, and LSE endometrial samples were collected.
Model validation group.The MV group consisted of 26 pairs of endometrial tissue samples from healthy volunteers at ESE and MSE phases.In addition, we included endometrial tissue samples collected from five healthy volunteers at LSE phase.Therefore, we sequenced 57 endometrial tissue samples from 31 volunteers (Table 1).The paired NC ESE and MSE samples were collected at the Nova Vita Clinic (Tallinn, Estonia), and the LSE samples were collected from Oulu University Hospital (Finland).All women had normal serum levels of progesterone, prolactin, and testosterone, negative screening results for sexually transmitted diseases, no uterine pathologies, at least one live-born child and no endometriosis or PCOS in the anamnesis.Tissue histology analysis revealed one MSE phase tissue sample belonging to PE phase, and one ESE sample had ambiguous histological morphology with minor similarities to the MSE samples.With these exceptions, the results of the histological evaluation were concordant with the time of the biopsy.
RIF study group.RIF group samples were obtained from women undergoing IVF at the Nova Vita Clinic in NC (n = 44, Table 1).The endometrial biopsies were collected for research purposes, and no frozen embryos were replaced in the same cycle.All RIF patients had undergone, on average, 3.8 previous unsuccessful IVF cycles with good-quality embryos, and the causes for infertility treatment were tubal (n = 15), male (n = 11), unknown (n = 8), endometriosis (n = 2), and other factors (n = 8).
RNA extraction from endometrial tissue.According to the manufacturer's protocol, endometrial tissue total RNA was extracted using miRNeasy or RNeasy Mini kit (Qiagen).DNase I treatment was performed on column using RNase-Free DNase Set (Qiagen).Purified RNA integrity number (RIN) and quantity were assigned with Bioanalyzer 2100 RNA Nano 6000 kit (Agilent Technologies) and Qubit RNA IQ Assay (Thermo Fisher Scientific).Samples with RIN ≥ 7 were considered eligible for further analysis.
First, gene expression signatures of 68 endometrial receptivity genes were analysed in the model training and development (MD) group samples (n = 63), consisting of both healthy volunteers and PCOS patients.Based on collected data, a continuous and quantitative three-stage (from pre-receptive to receptive to post-receptive) computational classification model was developed.Next, the model classification accuracy was validated on the model validation (MV) group samples (n = 57, including ESE, MSE, and LSE samples) of healthy women.Finally, the RIF group samples (n = 44, women with RIF in the natural cycle (NC) at MSE) were examined with the validated computational classification model.The outline of this study is presented in the Supplementary Fig. 1.

Figure 1 .
Figure 1.Illustrative schematic overview of beREADY endometrial receptivity biomarker analysis by TAC-seq technology.(A) Endometrial biopsy is the source of total RNA that contains a set of analysed biomarker genes.(B) The biopsy's visual quality control, total RNA extraction, and quality control (QC).(C) The set of selected biomarkers' RNA molecules in grey for the template of complementary DNA in green after oligo-T priming.(D) Biomarker-specific detection through DNA-DNA hybridisation with orange probes.The ligation joints the probe DNA molecules only in a perfect match.The blue arrows represent PCR primers introducing patientspecific barcodes that copy red UMI parts and orange biomarker regions for RNA sequencing.(E) Illumina RNA sequencing technology generates millions of reads per analysed sample.(F) The orange RNA sequencing reads represent raw data that includes technical PCR duplicates marked with red crosses.Further bioinformatic analysis recognises and removes the duplicates based on UMI-s and profiles the sample of interest naturally.The final step is a report.

Figure 2 .
Figure 2. Gene expression profiles of endometrial biomarker genes in samples of polycystic ovarian syndrome (PCOS) patients and healthy women.The average gene expression (per group) of all assayed and housekeepernormalised genes is presented for healthy and PCOS samples in the MD group.The lower and upper hinges of the boxplot correspond to the 25th and 75th percentiles.PE proliferative phase, ESE early-secretory phase, MSE mid-secretory phase, LSE late-secretory phase and MD model development.

Figure 3 .
Figure 3. PCA plot of the model development group detects distinct transcriptional profiles of endometrial phases.The UMI-corrected counts were normalised with the geometric mean of housekeepers and scaled.PE proliferative phase, ESE early-secretory phase, MSE mid-secretory phase, LSE late-secretory phase, PCA principal component analysis and UMI unique molecular identifier.

Figure 4 .
Figure 4. beREADY model output probabilities for model training and development group (MD) samples that belong to pre-receptive, receptive and post-receptive groups.The dashed lines represent intermediary groups as early-receptive and late-receptive decision boundaries, which are not detected in this analysis step.(A) The clustering between pre-receptive and receptive groups.Proliferative samples are marked with an asterisk.(B) The clustering between receptive and post-receptive groups.

Figure 5 .
Figure 5.A focused analysis of the model validation (MV) samples, revealing early-receptive samples in mid-secretory group.Each point on this plot represents the probability of belonging to the given class after the first cluster distancing.The colours represent the final prediction class for given samples.(A) Comparative pre-receptive and receptive group analysis revealed the intermediary early-receptive class shown in boundaries and positioned between dashed lines.(B) Pair-wise receptive and post-receptive group analysis confirmed five post-receptive samples shown in classification boundaries represented by dashed lines. https://doi.org/10.1038/s41598-023-40991-z

Table 1 .
General characteristics of study participants.BMI body mass index, RIF recurrent implantation failure, SD standard deviation.*Paired samples obtained from the same natural cycle in mid-secretory phase and early-secretory phase groups.Group description Model training and development group (MD) Model validation group (MV) RIF study group (RIF) Healthy (n = 35) PCOS (n = 39) Healthy (n = 31)* RIF (n = 44)