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Results: 4

1.

M(3): an improved SNP calling algorithm for Illumina BeadArray data.

Li G, Gelernter J, Kranzler HR, Zhao H.

Bioinformatics. 2012 Feb 1;28(3):358-65. doi: 10.1093/bioinformatics/btr673. Epub 2011 Dec 8.

PMID:
22155947
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

CNV discovery using SNP genotyping arrays.

Yau C, Holmes CC.

Cytogenet Genome Res. 2008;123(1-4):307-12. doi: 10.1159/000184722. Epub 2009 Mar 11. Review.

PMID:
19287169
[PubMed - indexed for MEDLINE]
3.

Quality control for genome-wide association studies.

Gondro C, Lee SH, Lee HK, Porto-Neto LR.

Methods Mol Biol. 2013;1019:129-47. doi: 10.1007/978-1-62703-447-0_5. Review.

PMID:
23756889
[PubMed - indexed for MEDLINE]
4.

Closing the genotype-phenotype gap. Findings from the section on bioinformatics.

Yip YL; Section Editor for the IMIA Yearbook Section on Bioinformatics.

Yearb Med Inform. 2010:82-5. Review.

PMID:
20938577
[PubMed - indexed for MEDLINE]

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