Short-read Sequencing
Short-Read Sequencing is a genome sequencing methodology that generates highly accurate sequence reads of relatively short length, typically ranging from 50 to 300 base pairs, by massively parallel sequencing of fragmented DNA templates to enable high-throughput reconstruction of genomic sequences.
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Publications per year
2017–2026
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Fast and accurate short read alignment with Burrows–Wheeler transform
Heng Li, Richard Durbin · Bioinformatics · 2009 · 62.8K citations · Full text
Model-based Analysis of ChIP-Seq (MACS)
Yong Zhang, Tao Liu, Clifford A. Meyer et al. · Genome biology · 2008 · 19.9K citations · Full text
Minimap2: pairwise alignment for nucleotide sequences
Heng Li · Bioinformatics · 2018 · 16.8K citations · Full text
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National Human Genome Research Institute, United States
17 publications · 2.1K citations
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Wellcome Sanger Institute
Cambridge, United Kingdom
33 h-index
169 publications
165.7K citations

Howard Hughes Medical Institute
Chevy Chase, United States
31 h-index
99 publications
31.5K citations
University of Washington
Seattle, United States
31 h-index
185 publications
28.7K citations
Stanford University
Stanford, United States
29 h-index
152 publications
33.3K citations

Broad Institute
Cambridge, United States
29 h-index
125 publications
70.2K citations
Pacific Biosciences (United States)
Menlo Park, United States
27 h-index
85 publications
11.3K citations

Johns Hopkins University
Baltimore, United States
27 h-index
127 publications
45K citations
Harvard University
Cambridge, United States
26 h-index
116 publications
70K citations
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89 publications · 155.6K citations
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GR · 49 publications · 14.5K citations
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50 publications · 5.9K citations
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54 publications · 5.7K citations
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63 publications · 4.2K citations
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