SNPnexus: assessing the functional relevance of genetic variation to facilitate the promise of precision medicine.

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SNPnexus: assessing the functional relevance of genetic variation to facilitate the promise of precision medicine.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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SNPnexus: assessing the functi ...... promise of precision medicine.

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SNPnexus: assessing the functi ...... promise of precision medicine.

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SNPnexus: assessing the functi ...... promise of precision medicine.

@en

SNPnexus: assessing the functi ...... promise of precision medicine.

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SNPnexus: assessing the functi ...... promise of precision medicine.

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SNPnexus: assessing the functi ...... promise of precision medicine.

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P1476

SNPnexus: assessing the functi ...... promise of precision medicine.

@en

P2093

Abu Z Dayem Ullah

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Ai Nagano

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Claude Chelala

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Jorge Oscanoa

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Nicholas R Lemoine

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P2860

An integrated encyclopedia of DNA elements in the human genome

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

dbSNP: the NCBI database of genetic variation

Analysis of protein-coding genetic variation in 60,706 humans

ClinVar: public archive of interpretations of clinically relevant variants

A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3

A general framework for estimating the relative pathogenicity of human genetic variants

The genetic association database

Tabix: fast retrieval of sequence features from generic TAB-delimited files.

FunSeq2: a framework for prioritizing noncoding regulatory variants in cancer

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W109-W113

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scholarly article

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10.1093/NAR/GKY399

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English

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P478

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Jun Wang

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2018-07-01T00:00:00Z

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29757393

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6030955

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