Research graph
References from Novel scripts for improved annotation and selection of variants from whole exome sequencing in cancer research. Local targets link to admitted publications; unresolved targets remain external evidence.
Fast and accurate short read alignment with Burrows–Wheeler transform
10.1093/bioinformatics/btp324 · 2009 · External reference
10.1038/ng.806
10.1038/ng.806 · External reference
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples
10.1038/nbt.2514 · 2013 · External reference
The human genome browser at UCSC
10.1101/gr.229102.articlepublishedonlinebeforeprintinmay2002 · 2002 · External reference
dbSNP: the NCBI database of genetic variation
10.1093/nar/29.1.308 · 2001 · External reference
COSMIC: mining complete cancer genomes in the catalogue of somatic mutations in cancer
10.1093/nar/gkq929 · 2011 · External reference
BioGPS: an extensible and customizable portal for querying and organizing gene annotation resources
10.1186/gb-2009-10-11-r130 · 2008 · External reference
Gene-disease network analysis reveals functional modules in mendelian, complex and environmental diseases
2010 · External reference
10.1093/nar/gkq603
10.1093/nar/gkq603 · External reference
Deriving the consequences of genomic variants with the ensembl API and SNP effect predictor
2010 · External reference
A method and server for predicting damaging missense mutations
10.1038/nmeth0410-248 · 2010 · External reference
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
10.1038/nprot.2009.86 · 2008 · External reference
Nature and nurture: a case of transcending haematological pre-malignancies in a pair of monozygotic twins adding possible clues on the pathogenesis of B-cell proliferations
10.1111/bjh.13305 · 2015 · External reference
