(Q38400823)

2 September 2017

CGtag: complete genomics toolkit and annotation in a cloud-based Galaxy (English)

1 reference

2 September 2017

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3

Mattias de Hollander

1 reference

2 September 2017

1

Saskia Hiltemann

1 reference

2 September 2017

Hailiang Mei

2

1 reference

2 September 2017

Ivo Palli

4

1 reference

2 September 2017

Peter van der Spek

5

1 reference

2 September 2017

Guido Jenster

6

1 reference

2 September 2017

Andrew Stubbs

7

1 reference

2 September 2017

24 January 2014

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2 September 2017

1 reference

2 September 2017

3

1 reference

2 September 2017

1

1 reference

2 September 2017

1

1 reference

https://scigraph.springernature.com/pub.10.1186/2047-217x-3-1

2 September 2017

0 references

cites work

Huvariome: a web server resource of whole genome next-generation sequencing allelic frequencies to aid in pathological candidate gene selection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3905657

Predicting the functional impact of protein mutations: application to cancer genomics

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3905657

FusionMap: detecting fusion genes from next-generation sequencing data at base-pair resolution

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3905657

Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3905657

Galaxy CloudMan: delivering cloud compute clusters

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3905657

Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3905657

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3905657

Galaxy: a web-based genome analysis tool for experimentalists

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3905657

Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3905657

Galaxy: a platform for interactive large-scale genome analysis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3905657

Boston type craniosynostosis: report of a second mutation in MSX2.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3905657

iFUSE: integrated fusion gene explorer

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3905657

Complex craniosynostosis is associated with the 2p15p16.1 microdeletion syndrome

31 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F2047-217X-3-1

21 January 2018

Identifiers

DOI

10.1186/2047-217X-3-1

1 reference

Dimensions Publication ID

2 September 2017

0 references

1 reference

2 September 2017

1 reference