The DOI matches its Crossref record; 13 of the 14 references it cites were found in a registry or an index.
From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline
Open accessAbstract
This unit describes how to use BWA and the Genome Analysis Toolkit (GATK) to map genome sequencing data to a reference and produce high‐quality variant calls that can be used in downstream analyses. The complete workflow includes the core NGS data‐processing steps that are necessary to make the raw data suitable for analysis by the GATK, as well as the key methods involved in variant discovery using the GATK. Curr. Protoc. Bioinform . 43:11.10.1‐11.10.33. © 2013 by John Wiley & Sons, Inc.
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“The best practices recommended by the Broad Institute for variant calling were then followed (Van der Auwera et al., 2013).”
From Loss of epigenetic information as a cause of mammalian aging (2023) · cites this paper as Van der Auwera et al., 2013
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Metadata
- Authors
- Van der Auwera, G. A., Carneiro, M. O., Hartl, C., Poplin, R., del Angel, G., Levy‐Moonshine, A., Jordan, T., Shakir, K., Roazen, D., Thibault, J., Banks, E., Garimella, K. V., Altshuler, D., Gabriel, S., & DePristo, M. A.
- Affiliations
- Genome Sequencing and Analysis Group Broad Institute Cambridge Massachusetts
- Broad Institute (US)
- Centre for Human Genetics (GB)
- ORCID
- Venue
- Current Protocols in Bioinformatics
- Publisher
- Wiley
- Published
- 2013-10
- Volume
- 43
- Issue
- 1
- Pages
- 11.10.1-11.10.33
- ISSN
- 1934-3396 (ISSN-L)
- 1934-340X
- PMC
- PMC4243306
- OpenAlex
- W1919257374
- Cited by
- 6,687
- References
- 14
- Citations by year
- 2026: 342 · 2025: 559 · 2024: 677 · 2023: 662 · 2022: 729 · 2021: 877 · 2020: 716 · 2019: 648 · 2018: 528 · 2017: 416 · 2016: 293 · 2015: 168 · 2014: 60 · 2013: 2
- FWCI
- 78.15
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Current Protocols in Bioinformatics (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Human Genome Research Institute (U54HG003067, U01HG006569)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genetics, Bioinformatics, and Biomedical Research
- Keywords
- variant calling, GATK, BWA, genome alignment, next-generation sequencing data processing, variant discovery, reference genome mapping, bioinformatics pipeline
- MeSH terms
- Calibration, Haploidy, Haplotypes, Humans, Software, Genetic Variation, Genome, Human, Sequence Alignment, Polymorphism, Single Nucleotide, Databases, Genetic, Molecular Sequence Annotation
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