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Sharing data between LSDBs and central repositories
scientific article
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instance of
scholarly article
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title
Sharing data between LSDBs and central repositories
(English)
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main subject
data sharing
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author
Paal S Andersen
object named as
Paal S Andersen
series ordinal
3
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Rolf H Sijmons
object named as
Rolf H Sijmons
series ordinal
2
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Ross Hardison
object named as
Ross C Hardison
series ordinal
8
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Mauno Vihinen
object named as
Mauno Vihinen
series ordinal
4
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Jacques S Beckmann
object named as
Jacques S Beckmann
series ordinal
5
0 references
author name string
Johan T den Dunnen
series ordinal
1
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Sandro Rossetti
series ordinal
6
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C Conover Talbot
series ordinal
7
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Sue Povey
series ordinal
9
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Richard G H Cotton
series ordinal
10
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language of work or name
English
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publication date
April 2009
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published in
Human Mutation
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volume
30
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page(s)
493-5
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issue
4
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cites work
Recommendations for locus-specific databases and their curation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4409810
retrieved
17 March 2017
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4409810
retrieved
17 March 2017
Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4409810
retrieved
3 June 2018
Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4409810
retrieved
3 June 2018
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4409810
retrieved
3 June 2018
PhenCode: connecting ENCODE data with mutations and phenotype
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4409810
retrieved
3 June 2018
Perspective on genes and mutations causing retinitis pigmentosa
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4409810
retrieved
3 June 2018
A survey of locus-specific database curation. Human Genome Variation Society
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.20977
retrieved
21 January 2018
Recommendations of the 2006 Human Variome Project meeting
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4409810
retrieved
27 November 2018
Identifiers
DOI
10.1002/HUMU.20977
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PMCID
4409810
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PubMed ID
19306393
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ResearchGate publication ID
24219764
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