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Supplement: mmc5.xlsx › UPS_somatic_mutations_filtered
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Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing.
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Human Mutation, 2015
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Supplement: HUMU-36-903-s001.zip › humu22825-sup-00010-Table_S13.xlsx › Sheet1
Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.
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Human Genomics, 2015
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The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
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Nucleic Acids Research, 2014
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Search for low penetrance alleles for colorectal cancer through a scan of 1467 non-synonymous SNPs in 2575 cases and 2707 controls with validation by kin-cohort analysis of 14 704 first-degree relatives.
Webb EL et al.
Human Molecular Genetics, 2006
Variants in the GH-IGF axis confer susceptibility to lung cancer.
Rudd MF et al.
Genome Research, 2006
Molecular genetic analysis of FIH-1, FH, and SDHB candidate tumour suppressor genes in renal cell carcinoma.
Morris MR et al.
Journal of Clinical Pathology, 2004
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