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Targeted sequencing of the human X chromosome exome.
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Europe PubMed Central
PMC publication ID
3154473
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
title
Targeted sequencing of the human X chromosome exome
(English)
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stated in
Europe PubMed Central
PMC publication ID
3154473
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
author
Amol C Shetty
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2
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Europe PubMed Central
PMC publication ID
3154473
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
Michael E Zwick
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5
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Michael E Zwick
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Europe PubMed Central
PMC publication ID
3154473
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
author name string
Kajari Mondal
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1
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Europe PubMed Central
PMC publication ID
3154473
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
Viren Patel
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3
1 reference
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Europe PubMed Central
PMC publication ID
3154473
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
David J Cutler
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4
1 reference
stated in
Europe PubMed Central
PMC publication ID
3154473
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
publication date
16 April 2011
1 reference
stated in
Europe PubMed Central
PMC publication ID
3154473
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
published in
Genomics
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Europe PubMed Central
PMC publication ID
3154473
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
volume
98
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Europe PubMed Central
PMC publication ID
3154473
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
issue
4
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stated in
Europe PubMed Central
PMC publication ID
3154473
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
page(s)
260-265
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stated in
Europe PubMed Central
PMC publication ID
3154473
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
cites work
Microarray oligonucleotide probe designer (MOPeD): A web service
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=3154473
retrieved
5 July 2018
Carrier testing for severe childhood recessive diseases by next-generation sequencing
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=3154473
retrieved
5 July 2018
The next-generation sequencing technology and application
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=3154473
retrieved
5 July 2018
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability
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=3154473
retrieved
5 July 2018
Genetics of early onset cognitive impairment
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=3154473
retrieved
5 July 2018
Whole exome capture in solution with 3 Gbp of data
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=3154473
retrieved
5 July 2018
Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.
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=3154473
retrieved
5 July 2018
Empirical evaluation of oligonucleotide probe selection for DNA microarrays
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=3154473
retrieved
5 July 2018
Microdroplet-based PCR enrichment for large-scale targeted sequencing
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=3154473
retrieved
5 July 2018
Enrichment of sequencing targets from the human genome by solution hybridization
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=3154473
retrieved
5 July 2018
Combining microarray-based genomic selection (MGS) with the Illumina Genome Analyzer platform to sequence diploid target regions
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=3154473
retrieved
5 July 2018
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
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=3154473
retrieved
5 July 2018
Lessons learnt from large-scale exon re-sequencing of the X chromosome
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=3154473
retrieved
5 July 2018
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
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=3154473
retrieved
5 July 2018
Next-generation DNA sequencing
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=3154473
retrieved
5 July 2018
Applications of next-generation sequencing technologies in functional genomics
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=3154473
retrieved
5 July 2018
Microarray-based mutation detection in the dystrophin gene
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=3154473
retrieved
5 July 2018
A second generation human haplotype map of over 3.1 million SNPs
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=3154473
retrieved
5 July 2018
Multiplex amplification of large sets of human exons
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=3154473
retrieved
5 July 2018
Direct selection of human genomic loci by microarray hybridization
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=3154473
retrieved
5 July 2018
Multiplex amplification of all coding sequences within 10 cancer genes by Gene-Collector
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=3154473
retrieved
5 July 2018
A haplotype map of the human genome
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=3154473
retrieved
5 July 2018
Direct genomic selection.
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=3154473
retrieved
5 July 2018
Multiplex amplification enabled by selective circularization of large sets of genomic DNA fragments
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=3154473
retrieved
5 July 2018
The DNA sequence of the human X chromosome
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=3154473
retrieved
5 July 2018
Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center.
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=3154473
retrieved
29 October 2018
A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families
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=3154473
retrieved
29 October 2018
Microarray-based genomic selection for high-throughput resequencing.
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=3154473
retrieved
29 October 2018
Overview: methods and applications for droplet compartmentalization of biology.
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=3154473
retrieved
29 October 2018
Identifiers
DOI
10.1016/J.YGENO.2011.04.004
1 reference
stated in
Europe PubMed Central
PMC publication ID
3154473
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
PMC publication ID
3154473
1 reference
stated in
Europe PubMed Central
PMC publication ID
3154473
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
PubMed publication ID
21524701
1 reference
stated in
Europe PubMed Central
PMC publication ID
3154473
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21524701%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 January 2020
ResearchGate publication ID
51081368
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