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| The sequence alignment/map format and SAMtools H Li, B Handsaker, A Wysoker, T Fennell, J Ruan, N Homer, G Marth, ... Bioinformatics 25 (16), 2078-2079, 2009 | 21821 | 2009 |
| Fast and accurate short read alignment with Burrows–Wheeler transform H Li, R Durbin bioinformatics 25 (14), 1754-1760, 2009 | 20844 | 2009 |
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| An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012 | 6018 | 2012 |
| Fast and accurate long-read alignment with Burrows–Wheeler transform H Li, R Durbin Bioinformatics 26 (5), 589-595, 2010 | 5554 | 2010 |
| The variant call format and VCFtools P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ... Bioinformatics 27 (15), 2156-2158, 2011 | 4154 | 2011 |
| 1000 Genome Project Data Processing Subgroup. 2009. The sequence alignment/map format and samtools H Li, B Handsaker, A Wysoker, T Fennell, J Ruan, N Homer, G Marth, ... Bioinformatics 25 (16), 2078-2079, 2009 | 3957 | 2009 |
| Accurate whole human genome sequencing using reversible terminator chemistry DR Bentley, S Balasubramanian, HP Swerdlow, GP Smith, J Milton, ... nature 456 (7218), 53, 2008 | 3581 | 2008 |
| The Pfam protein families database A Bateman, L Coin, R Durbin, RD Finn, V Hollich, S Griffiths‐Jones, ... Nucleic acids research 32 (suppl_1), D138-D141, 2004 | 3470 | 2004 |
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| Mapping short DNA sequencing reads and calling variants using mapping quality scores H Li, J Ruan, R Durbin Genome research 18 (11), 1851-1858, 2008 | 2918 | 2008 |
| Ensembl 2012 P Flicek, MR Amode, D Barrell, K Beal, S Brent, D Carvalho-Silva, ... Nucleic acids research 40 (D1), D84-D90, 2011 | 2800 | 2011 |
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Heng LiDana-Farber Cancer Institute & Harvard UniversityDirección de correo verificada de jimmy.harvard.edu
