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Genomics
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January 9, 2007
hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes
Philippe Lamesch, Ning Li, Stuart Milstein, et al.
Human Molecular Genetics
|
October 14, 2005
Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays
Alvaro Rada-Iglesias, Ola Wallerman, Christoph Koch, et al.
Database : the Journal of Biological Databases and Curation
|
February 19, 2016
Ensembl regulation resources
Daniel R Zerbino, Nathan Johnson, Thomas Juetteman, et al.
BMC Genetics
|
May 19, 2007
Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11
Sergey Nejentsev, Luc J Smink, Deborah Smyth, et al.
Cell
|
October 30, 2010
ATR-X syndrome protein targets tandem repeats and influences allele-specific expression in a size-dependent manner
Martin J Law, Karen M Lower, Hsiao P J Voon, et al.
Genome Research
|
June 15, 2007
The landscape of histone modifications across 1% of the human genome in five human cell lines
Christoph M Koch, Robert M Andrews, Paul Flicek, et al.
Nature
|
July 12, 2002
A first-generation linkage disequilibrium map of human chromosome 22
Elisabeth Dawson, Gonçalo R Abecasis, Suzannah Bumpstead, et al.
Genome Research
|
May 14, 2004
Complete MHC haplotype sequencing for common disease gene mapping
C Andrew Stewart, Roger Horton, Richard J N Allcock, et al.
Cell Reports
|
November 17, 2016
eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data
Charles E Breeze, Dirk S Paul, Jenny van Dongen, et al.
Nucleic Acids Research
|
November 16, 2020
Open Targets Platform: supporting systematic drug-target identification and prioritisation
David Ochoa, Andrew Hercules, Miguel Carmona, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 109) with videos related to
Sort By:
Page
of 11
Genomics
|
January 9, 2007
hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes
Philippe Lamesch, Ning Li, Stuart Milstein, et al.
Human Molecular Genetics
|
October 14, 2005
Binding sites for metabolic disease related transcription factors inferred at base pair resolution by chromatin immunoprecipitation and genomic microarrays
Alvaro Rada-Iglesias, Ola Wallerman, Christoph Koch, et al.
Database : the Journal of Biological Databases and Curation
|
February 19, 2016
Ensembl regulation resources
Daniel R Zerbino, Nathan Johnson, Thomas Juetteman, et al.
BMC Genetics
|
May 19, 2007
Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11
Sergey Nejentsev, Luc J Smink, Deborah Smyth, et al.
Cell
|
October 30, 2010
ATR-X syndrome protein targets tandem repeats and influences allele-specific expression in a size-dependent manner
Martin J Law, Karen M Lower, Hsiao P J Voon, et al.
Genome Research
|
June 15, 2007
The landscape of histone modifications across 1% of the human genome in five human cell lines
Christoph M Koch, Robert M Andrews, Paul Flicek, et al.
Nature
|
July 12, 2002
A first-generation linkage disequilibrium map of human chromosome 22
Elisabeth Dawson, Gonçalo R Abecasis, Suzannah Bumpstead, et al.
Genome Research
|
May 14, 2004
Complete MHC haplotype sequencing for common disease gene mapping
C Andrew Stewart, Roger Horton, Richard J N Allcock, et al.
Cell Reports
|
November 17, 2016
eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data
Charles E Breeze, Dirk S Paul, Jenny van Dongen, et al.
Nucleic Acids Research
|
November 16, 2020
Open Targets Platform: supporting systematic drug-target identification and prioritisation
David Ochoa, Andrew Hercules, Miguel Carmona, et al.
Page
of 11