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| == Required Reading == | | == Required Reading == |
| | | |
− | Browning SR, Browning BL (2007) Rapid and accurate haplotype phasing and | + | * Browning SR, Browning BL (2007) Rapid and accurate haplotype phasing and |
| missing-data inference for whole-genome association studies by use of localized | | missing-data inference for whole-genome association studies by use of localized |
| haplotype clustering. ''Am J Hum Genet.'' '''81''':1084-97. PMID: 17924348 | | haplotype clustering. ''Am J Hum Genet.'' '''81''':1084-97. PMID: 17924348 |
| | | |
− | Coventry A, Bull-Otterson LM, Liu X, Clark AG, Maxwell TJ, Crosby J, Hixson | + | * Coventry A, Bull-Otterson LM, Liu X, Clark AG, Maxwell TJ, Crosby J, Hixson |
| JE, Rea TJ, Muzny DM, Lewis LR, Wheeler DA, Sabo A, Lusk C, Weiss KG, Akbar H, | | JE, Rea TJ, Muzny DM, Lewis LR, Wheeler DA, Sabo A, Lusk C, Weiss KG, Akbar H, |
| Cree A, Hawes AC, Newsham I, Varghese RT, Villasana D, Gross S, Joshi V, | | Cree A, Hawes AC, Newsham I, Varghese RT, Villasana D, Gross S, Joshi V, |
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| explosive population growth. ''Nat Commun.'' '''1''':131. PMID: 21119644 | | explosive population growth. ''Nat Commun.'' '''1''':131. PMID: 21119644 |
| | | |
− | Delaneau O, Zagury JF, Marchini J (2013) Improved whole-chromosome phasing for | + | * Delaneau O, Zagury JF, Marchini J (2013) Improved whole-chromosome phasing for |
| disease and population genetic studies. ''Nat Methods.'' '''10''':5-6. PMID: 23269371 | | disease and population genetic studies. ''Nat Methods.'' '''10''':5-6. PMID: 23269371 |
| | | |
− | Howie B, Fuchsberger C, Stephens M, Marchini J, Abecasis GR (2012) Fast and accurate | + | * Howie B, Fuchsberger C, Stephens M, Marchini J, Abecasis GR (2012) Fast and accurate |
| genotype imputation in genome-wide association studies through pre-phasing. ''Nat | | genotype imputation in genome-wide association studies through pre-phasing. ''Nat |
| Genet.'' '''44''':955-9. PMID: 22820512 | | Genet.'' '''44''':955-9. PMID: 22820512 |
| | | |
− | Iqbal Z, Caccamo M, Turner I, Flicek P, McVean G (2012) De novo assembly and | + | * Iqbal Z, Caccamo M, Turner I, Flicek P, McVean G (2012) De novo assembly and |
| genotyping of variants using colored de Bruijn graphs. ''Nat Genet.'' '''44''':226-32. | | genotyping of variants using colored de Bruijn graphs. ''Nat Genet.'' '''44''':226-32. |
| PMID: 22231483 | | PMID: 22231483 |
| | | |
− | Jun G, Flickinger M, Hetrick KN, Romm JM, Doheny KF, Abecasis GR, Boehnke M, | + | * Jun G, Flickinger M, Hetrick KN, Romm JM, Doheny KF, Abecasis GR, Boehnke M, |
| Kang HM (2012) Detecting and estimating contamination of human DNA samples in | | Kang HM (2012) Detecting and estimating contamination of human DNA samples in |
| sequencing and array-based genotype data. ''Am J Hum Genet.'' '''91''':839-48. PMID: | | sequencing and array-based genotype data. ''Am J Hum Genet.'' '''91''':839-48. PMID: |
| 23103226 | | 23103226 |
| | | |
− | Li H, Ruan J, Durbin R (2008) Mapping short DNA sequencing reads and calling | + | * Li H, Ruan J, Durbin R (2008) Mapping short DNA sequencing reads and calling |
| variants using mapping quality scores. ''Genome Res.'' '''18''':1851-8. PMID: 18714091 | | variants using mapping quality scores. ''Genome Res.'' '''18''':1851-8. PMID: 18714091 |
| | | |
− | Li H, Durbin R (2009) Fast and accurate short read alignment with Burrows-Wheeler | + | * Li H, Durbin R (2009) Fast and accurate short read alignment with Burrows-Wheeler |
| transform. ''Bioinformatics.'' '''25''':1754-60. PMID: 19451168 | | transform. ''Bioinformatics.'' '''25''':1754-60. PMID: 19451168 |
| | | |
− | Li H, Durbin R (2011) Inference of human population history from individual | + | * Li H, Durbin R (2011) Inference of human population history from individual |
| whole-genome sequences. ''Nature.'' '''475''':493-6. PMID: 21753753 | | whole-genome sequences. ''Nature.'' '''475''':493-6. PMID: 21753753 |
| | | |
− | Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR (2010) MaCH: using sequence and | + | * Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR (2010) MaCH: using sequence and |
| genotype data to estimate haplotypes and unobserved genotypes. ''Genet Epidemiol.'' | | genotype data to estimate haplotypes and unobserved genotypes. ''Genet Epidemiol.'' |
| '''34''':816-34. PMID: 21058334 | | '''34''':816-34. PMID: 21058334 |
| | | |
− | Lin DY, Zeng D (2010) Meta-analysis of genome-wide association studies: no | + | * Lin DY, Zeng D (2010) Meta-analysis of genome-wide association studies: no |
| efficiency gain in using individual participant data. ''Genet Epidemiol.'' '''34''':60-6. | | efficiency gain in using individual participant data. ''Genet Epidemiol.'' '''34''':60-6. |
| PMID: 19847795 | | PMID: 19847795 |
| | | |
− | Wen X, Stephens M (2010) Using linear predictors to impute allele frequencies from | + | * Wen X, Stephens M (2010) Using linear predictors to impute allele frequencies from |
| summary or pooled genotype data. ''Ann Appl Stat.'' '''4''':1158-1182. PMID: 21479081 | | summary or pooled genotype data. ''Ann Appl Stat.'' '''4''':1158-1182. PMID: 21479081 |
| | | |
− | Zerbino DR, Birney E (2008) Velvet: algorithms for de novo short read assembly | + | * Zerbino DR, Birney E (2008) Velvet: algorithms for de novo short read assembly |
| using de Bruijn graphs. ''Genome Res.'' '''18''':821-9. PMID: 18349386 | | using de Bruijn graphs. ''Genome Res.'' '''18''':821-9. PMID: 18349386 |
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