Submitted by ja607 on
Title | A synthetic-diploid benchmark for accurate variant-calling evaluation. |
Publication Type | Journal Article |
Year of Publication | 2018 |
Authors | Li, H, Bloom, JM, Farjoun, Y, Fleharty, M, Gauthier, L, Neale, B, MacArthur, D |
Journal | Nat Methods |
Volume | 15 |
Issue | 8 |
Pagination | 595-597 |
Date Published | 2018 08 |
ISSN | 1548-7105 |
Keywords | Algorithms, Benchmarking, Cell Line, Tumor, Databases, Genetic, Diploidy, Female, Genetic Variation, Genome, Human, Homozygote, Humans, Hydatidiform Mole, Pregnancy, Synthetic Biology, Uterine Neoplasms, Whole Genome Sequencing |
Abstract | Existing benchmark datasets for use in evaluating variant-calling accuracy are constructed from a consensus of known short-variant callers, and they are thus biased toward easy regions that are accessible by these algorithms. We derived a new benchmark dataset from the de novo PacBio assemblies of two fully homozygous human cell lines, which provides a relatively more accurate and less biased estimate of small-variant-calling error rates in a realistic context. |
DOI | 10.1038/s41592-018-0054-7 |
Alternate Journal | Nat. Methods |
PubMed ID | 30013044 |
PubMed Central ID | PMC6341484 |
Grant List | R01 HG010040 / HG / NHGRI NIH HHS / United States U01 HG009088 / HG / NHGRI NIH HHS / United States U54 DK105566 / DK / NIDDK NIH HHS / United States |