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M Brudno

Showing results (1-10 of 7) with videos related to

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Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|January 31, 2008
FRESCO: flexible alignment with rectangle scoring schemesA V Dalca, M Brudno
Nucleic Acids Research|December 11, 1999
ASDB: database of alternatively spliced genesI Dralyuk, M Brudno, M S Gelfand, et al.
Nucleic Acids Research|May 29, 2001
Computational analysis of candidate intron regulatory elements for tissue-specific alternative pre-mRNA splicingM Brudno, M S Gelfand, S Spengler, et al.
Genome Research|September 14, 2000
Active conservation of noncoding sequences revealed by three-way species comparisonsI Dubchak, M Brudno, G G Loots, et al.
Bioinformatics (Oxford, England)|February 13, 2001
VISTA : visualizing global DNA sequence alignments of arbitrary lengthC Mayor, M Brudno, J R Schwartz, et al.
Clinical Epigenetics|July 18, 2019
Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variantsM T Siu, D T Butcher, A L Turinsky, et al.
Nature Communications|December 23, 2015
NSD1 mutations generate a genome-wide DNA methylation signatureS Choufani, C Cytrynbaum, B H Y Chung, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|January 31, 2008
FRESCO: flexible alignment with rectangle scoring schemesA V Dalca, M Brudno
Nucleic Acids Research|December 11, 1999
ASDB: database of alternatively spliced genesI Dralyuk, M Brudno, M S Gelfand, et al.
Nucleic Acids Research|May 29, 2001
Computational analysis of candidate intron regulatory elements for tissue-specific alternative pre-mRNA splicingM Brudno, M S Gelfand, S Spengler, et al.
Genome Research|September 14, 2000
Active conservation of noncoding sequences revealed by three-way species comparisonsI Dubchak, M Brudno, G G Loots, et al.
Bioinformatics (Oxford, England)|February 13, 2001
VISTA : visualizing global DNA sequence alignments of arbitrary lengthC Mayor, M Brudno, J R Schwartz, et al.
Clinical Epigenetics|July 18, 2019
Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variantsM T Siu, D T Butcher, A L Turinsky, et al.
Nature Communications|December 23, 2015
NSD1 mutations generate a genome-wide DNA methylation signatureS Choufani, C Cytrynbaum, B H Y Chung, et al.
Pageof 1