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Genome Medicine
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June 10, 2017
brain-coX: investigating and visualising gene co-expression in seven human brain transcriptomic datasets
Saskia Freytag, Rosemary Burgess, Karen L Oliver, et al.
Plos Genetics
|
May 24, 2018
Identity-by-descent analyses for measuring population dynamics and selection in recombining pathogens
Lyndal Henden, Stuart Lee, Ivo Mueller, et al.
BMC Bioinformatics
|
September 26, 2015
Systematic noise degrades gene co-expression signals but can be corrected
Saskia Freytag, Johann Gagnon-Bartsch, Terence P Speed, et al.
F1000Research
|
August 28, 2024
UKB.COVID19: an R package for UK Biobank COVID-19 data processing and analysis
Longfei Wang, Victoria E Jackson, Liam G Fearnley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 19, 2023
Exploring THAP11 Repeat Expansion beyond Chinese-Ancestry Cohorts: An Examination of 1000 Genomes and UK Biobank Data
Liam G Fearnley, Haloom Rafehi, Mark F Bennett, et al.
F1000Research
|
January 5, 2019
Comparison of clustering tools in R for medium-sized 10x Genomics single-cell RNA-sequencing data
Saskia Freytag, Luyi Tian, Ingrid Lönnstedt, et al.
Bioinformatics (Oxford, England)
|
November 9, 2018
dtangle: accurate and robust cell type deconvolution
Gregory J Hunt, Saskia Freytag, Melanie Bahlo, et al.
Communications Biology
|
November 19, 2025
Identification of novel vertebral development factors through UK Biobank candidate gene search and body imaging analysis
Zhuopin Sun, Jiru Han, Liam G Fearnley, et al.
American Journal of Medical Genetics. Part A
|
August 30, 2007
Keipert syndrome (Nasodigitoacoustic syndrome) is X-linked and maps to Xq22.2-Xq28
David J Amor, Hans-Henrik M Dahl, Melanie Bahlo, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 25, 2007
Probabilistic analysis of recessive mutagenesis screen strategies
Jeremy D Silver, Douglas J Hilton, Melanie Bahlo, et al.
Page
of 28
Search research articles
Search
Showing results (11-20 of 280) with videos related to
Sort By:
Page
of 28
Genome Medicine
|
June 10, 2017
brain-coX: investigating and visualising gene co-expression in seven human brain transcriptomic datasets
Saskia Freytag, Rosemary Burgess, Karen L Oliver, et al.
Plos Genetics
|
May 24, 2018
Identity-by-descent analyses for measuring population dynamics and selection in recombining pathogens
Lyndal Henden, Stuart Lee, Ivo Mueller, et al.
BMC Bioinformatics
|
September 26, 2015
Systematic noise degrades gene co-expression signals but can be corrected
Saskia Freytag, Johann Gagnon-Bartsch, Terence P Speed, et al.
F1000Research
|
August 28, 2024
UKB.COVID19: an R package for UK Biobank COVID-19 data processing and analysis
Longfei Wang, Victoria E Jackson, Liam G Fearnley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 19, 2023
Exploring THAP11 Repeat Expansion beyond Chinese-Ancestry Cohorts: An Examination of 1000 Genomes and UK Biobank Data
Liam G Fearnley, Haloom Rafehi, Mark F Bennett, et al.
F1000Research
|
January 5, 2019
Comparison of clustering tools in R for medium-sized 10x Genomics single-cell RNA-sequencing data
Saskia Freytag, Luyi Tian, Ingrid Lönnstedt, et al.
Bioinformatics (Oxford, England)
|
November 9, 2018
dtangle: accurate and robust cell type deconvolution
Gregory J Hunt, Saskia Freytag, Melanie Bahlo, et al.
Communications Biology
|
November 19, 2025
Identification of novel vertebral development factors through UK Biobank candidate gene search and body imaging analysis
Zhuopin Sun, Jiru Han, Liam G Fearnley, et al.
American Journal of Medical Genetics. Part A
|
August 30, 2007
Keipert syndrome (Nasodigitoacoustic syndrome) is X-linked and maps to Xq22.2-Xq28
David J Amor, Hans-Henrik M Dahl, Melanie Bahlo, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 25, 2007
Probabilistic analysis of recessive mutagenesis screen strategies
Jeremy D Silver, Douglas J Hilton, Melanie Bahlo, et al.
Page
of 28