Associated Papers
Exome-Sequence Analyses of Four Multi-Incident Multiple Sclerosis Families.
Zrzavy T et al.
Genes, 2020
32854198 (PubMed )
Supplement: genes-11-00988-s001.pdf
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A2-A04Y-01A.domain
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.
Brownstein CA et al.
Genome Biology, 2014
24667040 (PubMed )
Supplement: gb-2014-15-3-r53-S3.pdf
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