A beginners guide to SNP calling from high-throughput DNA-sequencing data-Reference-Cited by-同舟云学术

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A beginners guide to SNP calling from high-throughput DNA-sequencing data

Published:2012-08-11 Issue:10 Volume:131 Page:1541-1554
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Altmann André,Weber Peter,Bader Daniel,Preuß Michael,Binder Elisabeth B.,Müller-Myhsok Bertram

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-012-1213-z.pdf

Reference57 articles.

1. Abeel T, Van Parys T, Saeys Y, Galagan J, Van de Peer Y (2012) GenomeView: a next-generation genome browser. Nucleic Acids Res 40:e12

2. Bansal V, Libiger O, Torkamani A, Schork NJ (2010) Statistical analysis strategies for association studies involving rare variants. Nat Rev Genet 11:773–785

3. Barski A, Cuddapah S, Cui K, Roh TY, Schones DE, Wang Z, Wei G, Chepelev I, Zhao K (2007) High-resolution profiling of histone methylations in the human genome. Cell 129:823–837

4. Browning BL, Yu Z (2009) Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies. Am J Hum Genet 85:847–861

5. Burrows M, Wheeler DJ (1994) A block-sorting lossless data compression algorithm. Technical Report Digital Equipment Corporation, Palo Alto

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