Assessing the reproducibility, accuracy and utility of massively parallel DNA sequencing platforms remains an ongoing challenge. Here the Association of Biomolecular Resource Facilities (ABRF) Next-Generation Sequencing Study benchmarks the performance of a set of sequencing instruments (HiSeq/NovaSeq/paired-end 2 × 250-bp chemistry, Ion S5/Proton, PacBio circular consensus sequencing (CCS), Oxford Nanopore Technologies PromethION/MinION, BGISEQ-500/MGISEQ-2000 and GS111) on human and bacterial reference DNA samples. Among short-read instruments, HiSeq 4000 and X10 provided the most consistent, highest genome coverage, while BGI/MGISEQ provided the lowest sequencing error rates. The long-read instrument PacBio CCS had the highest reference-based mapping rate and lowest non-mapping rate. The two long-read platforms PacBio CCS and PromethION/MinION showed the best sequence mapping in repeat-rich areas and across homopolymers. NovaSeq 6000 using 2 × 250-bp read chemistry was the most robust instrument for capturing known insertion/deletion events. This study serves as a benchmark for current genomics technologies, as well as a resource to inform experimental design and next-generation sequencing variant calling.
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The genome sequences in this study are available as EBV-immortalized B lymphocyte cell lines (from Coriell) as well as from DNA (from Coriell and NIST). The data in this study were derived from the batch of DNA from the NIST Reference Materials. All data generated within this study from these genomes are publicly available on the NCBI Sequence Read Archive under the BioProject PRJNA646948, within accessions SRR12898279–SRR12898354.
All code used within this study is publicly available at https://www.github.com/jfoox/abrfngs2. This repository includes directories containing scripts for primary analyses such as alignment and variant calling (SLURM/), shell scripts to perform post-processing calculations (bin/) and R scripts used to create figures (Rmds/). All tables used to generate figures are provided in a tables/ directory.
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We thank Illumina and ThermoFisher for providing reagents allowing the study to take place. We also thank NIST for providing the GIAB DNA samples necessary to carry out the study. We acknowledge the HudsonAlpha Institute of Biotechnology for expert assistance in Illumina DNA library preparation. The Association of Biomolecular Resource Facilities (ABRF) also provided funding, logistical support and project oversight. We thank the ABRF NGS Study members, who contributed to the design and execution of this project. We are particularly grateful for the assistance provided by multiple core facilities spending their own time and resources to participate in this research. We thank the Epigenomics Core Facility and Scientific Computing Unit at Weill Cornell Medicine, as well as the Starr Cancer Consortium (I9-A9-071), and acknowledge funding from the Irma T. Hirschl and Monique Weill-Caulier Charitable Trusts, Bert L and N Kuggie Vallee Foundation, the WorldQuant Foundation, The Pershing Square Sohn Cancer Research Alliance, NASA (NNX14AH50G, NNX17AB26G), the National Institutes of Health (R25EB020393, R01NS076465, R01AI125416, R01ES021006, 1R21AI129851, 1R01MH117406), the Bill and Melinda Gates Foundation (OPP1151054), TRISH (NNX16AO69A:0107, NNX16AO69A:0061), the Leukemia and Lymphoma Society grants (LLS 9238-16, Mak, LLS-MCL-982, Chen-Kiang) and the Alfred P. Sloan Foundation (G-2015-13964). Certain commercial equipment, instruments or materials are identified to adequately specify experimental conditions or reported results. Such identification implies neither recommendation nor endorsement by the National Institute of Standards and Technology, nor does it imply that the equipment, instruments or materials identified are necessarily the best available for the purpose. F.J.S. and M.M. are supported by the NIH (UM1 HG008898).
G.P.S. is employed by Illumina Inc. X.Z., W.Z., F.T., Y.Z. and H.L are employees of MGI Inc. All other authors declare no competing interests.
Peer review information Nature Biotechnology thanks the anonymous reviewers for their contribution to the peer review of this work.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
(a) The insert Size distribution of every replicate, stratified by sequencing instrument. (b) The percentage of total reads that were mapped to decoy contigs within the GRCh38 reference genome.
Heatmap showing the distribution of read counts per library (rows) by GC content (columns) across human whole genome and exome samples. Read count values are normalized by total reads per replicate, such that a value of 1 matches maximum value for a given replicate. Annotation tracks on the right indicate the sequencing platform and cell line genome for that replicate.
Comparisons for every platform within each UCSC RepeatMasker region. Blue bars indicate >50% of shared sites are better represented in the given platform (column) versus all other platforms (rows). Red bars indicate that the other platform out-covered the given platform.
Precision and sensitivity scores as derived from rtg vcfeval analysis, stratified by regions in (a) the CLINVAR database and (b) the OMIM database. For each of the cell lines, genes from each database were overlapped with high confidence regions for variant calling. (c) Scores stratified by regions in the exome, as defined by the AmpliSeq target capture regions file. For each of the cell lines, exomic regions were overlapped with high confidence regions for variant calling.
Heatmap of genotype (GT) of variant alleles on chromosome 1, across all human replicates across within sequencing platforms, as measured against the Genome in a Bottle high confidence variant call sets for each genome. Heterozygous variant alleles are shaded in orange (0.5), homozygous variants in red (1), missing data in blue (0), and inapplicable sites (sites outside of the GIAB high confidence region in one cell line but present in another) in gray. Hierarchical clustering reveals strong grouping by cell line, followed by less clear grouping within platforms and inter- and intra-lab replicates.
UpSet intersections of Mendelian violations. Each plot is stratified by variant type (SNPs on top, followed by INDELs; INS_5 = insertions 0-5 bp in size, INS_6to15 = insertions 6 to 15 bp in size, INS_15 = insertions >15 bp in size; same for deletions, ‘DEL’). Events were recorded within high confidence regions for the Ashkenazi Son (HG002).
Comparison between the identified SVs in the six replicates from long-read sequencing instruments, showing agreement of 6,980 SVs between samples (green column).
Coverage, insert size, and read length mean and standard deviation across total SVs in sequencing runs.
(a) Insights into SV variability by caller. First the strategy used to examine SV caller variability after stratifying for platforms, replicates and centers variability; next the SV call set sizes and overlap with the GIAB SV call set for the SV caller variability set of HG002; finally the types and sizes of SVs in the SV caller variability set of HG002 (translocations are set to size 50 by default in the SURVIVOR parameters for visualization purposes). (b) Insights into SV variability by platform. Diagrams utilize sequencing runs from HiSeqX10, HiSeq2000 and HiSeq4000 while the final two characterize all platforms available. First the strategy used to examine platform variability after stratifying for SV callers, centers and replicates variability; next, SV call set sizes and overlaps with the GIAB SV call set for the platform variability SV call set of HG002; next, types and sizes of SVs in the platform variability SV call set of HG002. Final two panels include HiSeqX10, HiSeq2000, HiSeq4000, NovaSeq, BGI and MGI for visualization purposes. The NovaSeq, BGI and MGI SV call sets were not integrated into the analyses strategy because sequencing runs with replicates for each sample at different centers on different platforms were not available. On top, SV call set sizes and overlap with the GIAB SV call set for the platform variability SV call set of HG002. Below, types and sizes of SVs in the platform variability SV call set of HG002. (Translocations are set to size 50 by default in the SURVIVOR parameters for visualization purposes).
(a) Heatmap showing the distribution of read counts per library (rows) by GC content (columns) across bacterial genomes and the metagenomic mixtrue. Read count values are normalized by total reads per replicate, such that a value of 1 matches maximum value for a given replicate. Annotation tracks on the right indicate the sequencing platform and cell line genome for that replicate. (b) Calculations of entropy per genome/metagenomic mixture. Entropy was measured across all GC windows for all replicates for a given sample, rowSums(-(p * log(p)).
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Foox, J., Tighe, S.W., Nicolet, C.M. et al. Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study. Nat Biotechnol 39, 1129–1140 (2021). https://doi.org/10.1038/s41587-021-01049-5
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