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Proceedings of the National Academy of Sciences of the United States of America
|
March 20, 2013
Whole-genome haplotyping by dilution, amplification, and sequencing
Fiona Kaper, Sajani Swamy, Brandy Klotzle, et al.
Frontiers in Plant Science
|
March 30, 2018
Sequencing and Analysis of <i>Strobilanthes cusia</i> (Nees) Kuntze Chloroplast Genome Revealed the Rare Simultaneous Contraction and Expansion of the Inverted Repeat Region in Angiosperm
Haimei Chen, Junjie Shao, Hui Zhang, et al.
Genome Research
|
October 21, 2014
In vitro, long-range sequence information for de novo genome assembly via transposase contiguity
Andrew Adey, Jacob O Kitzman, Joshua N Burton, et al.
Journal of Virology
|
August 22, 2008
Minority human immunodeficiency virus type 1 variants in antiretroviral-naive persons with reverse transcriptase codon 215 revertant mutations
Yumi Mitsuya, Vici Varghese, Chunlin Wang, et al.
Immunogenetics
|
July 23, 2015
Very long haplotype tracts characterized at high resolution from HLA homozygous cell lines
Paul J Norman, Steve J Norberg, Neda Nemat-Gorgani, et al.
Plos One
|
November 13, 2012
mRNA-Seq of single prostate cancer circulating tumor cells reveals recapitulation of gene expression and pathways found in prostate cancer
Gordon M Cann, Zulfiqar G Gulzar, Samantha Cooper, et al.
Nature Biotechnology
|
May 6, 2003
Multiplexed genotyping with sequence-tagged molecular inversion probes
Paul Hardenbol, Johan Banér, Maneesh Jain, et al.
Human Molecular Genetics
|
August 7, 2009
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma
Mehrnaz Narooie-Nejad, Seyed Hassan Paylakhi, Seyedmehdi Shojaee, et al.
Human Mutation
|
October 15, 2008
Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease
Balaji S Srinivasan, Jaleh Doostzadeh, Farnaz Absalan, et al.
Scientific Reports
|
January 9, 2014
Mutation in ST6GALNAC5 identified in family with coronary artery disease
Kolsoum InanlooRahatloo, Amir Farhang Zand Parsa, Klaus Huse, et al.
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Search research articles
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Showing results (41-50 of 72) with videos related to
Sort By:
Page
of 8
Proceedings of the National Academy of Sciences of the United States of America
|
March 20, 2013
Whole-genome haplotyping by dilution, amplification, and sequencing
Fiona Kaper, Sajani Swamy, Brandy Klotzle, et al.
Frontiers in Plant Science
|
March 30, 2018
Sequencing and Analysis of <i>Strobilanthes cusia</i> (Nees) Kuntze Chloroplast Genome Revealed the Rare Simultaneous Contraction and Expansion of the Inverted Repeat Region in Angiosperm
Haimei Chen, Junjie Shao, Hui Zhang, et al.
Genome Research
|
October 21, 2014
In vitro, long-range sequence information for de novo genome assembly via transposase contiguity
Andrew Adey, Jacob O Kitzman, Joshua N Burton, et al.
Journal of Virology
|
August 22, 2008
Minority human immunodeficiency virus type 1 variants in antiretroviral-naive persons with reverse transcriptase codon 215 revertant mutations
Yumi Mitsuya, Vici Varghese, Chunlin Wang, et al.
Immunogenetics
|
July 23, 2015
Very long haplotype tracts characterized at high resolution from HLA homozygous cell lines
Paul J Norman, Steve J Norberg, Neda Nemat-Gorgani, et al.
Plos One
|
November 13, 2012
mRNA-Seq of single prostate cancer circulating tumor cells reveals recapitulation of gene expression and pathways found in prostate cancer
Gordon M Cann, Zulfiqar G Gulzar, Samantha Cooper, et al.
Nature Biotechnology
|
May 6, 2003
Multiplexed genotyping with sequence-tagged molecular inversion probes
Paul Hardenbol, Johan Banér, Maneesh Jain, et al.
Human Molecular Genetics
|
August 7, 2009
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma
Mehrnaz Narooie-Nejad, Seyed Hassan Paylakhi, Seyedmehdi Shojaee, et al.
Human Mutation
|
October 15, 2008
Whole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson disease
Balaji S Srinivasan, Jaleh Doostzadeh, Farnaz Absalan, et al.
Scientific Reports
|
January 9, 2014
Mutation in ST6GALNAC5 identified in family with coronary artery disease
Kolsoum InanlooRahatloo, Amir Farhang Zand Parsa, Klaus Huse, et al.
Page
of 8