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Michael Wigler

Showing results (51-60 of 71) with videos related to

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Cell|November 18, 2008
An oncogenomics-based in vivo RNAi screen identifies tumor suppressors in liver cancerLars Zender, Wen Xue, Johannes Zuber, et al.
Human Genetics|August 28, 2013
The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart diseaseDorothy Warburton, Michael Ronemus, Jennie Kline, et al.
Communications Biology|September 2, 2021
Rates of contributory de novo mutation in high and low-risk autism familiesSeungtai Yoon, Adriana Munoz, Boris Yamrom, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 2012
A cluster of cooperating tumor-suppressor gene candidates in chromosomal deletionsWen Xue, Thomas Kitzing, Stephanie Roessler, et al.
Genome Research|September 17, 2003
Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variationRobert Lucito, John Healy, Joan Alexander, et al.
Science (New York, N.Y.)|July 27, 2004
Large-scale copy number polymorphism in the human genomeJonathan Sebat, B Lakshmi, Jennifer Troge, et al.
Genome Biology|September 27, 2025
Hybrid BAG-seq: DNA and RNA from the same single nucleus reveals interactions between genomic and transcriptomic landscapes in human tumor samplesSiran Li, Joan Alexander, Jude Kendall, et al.
Nature Protocols|November 18, 2016
Indel variant analysis of short-read sequencing data with ScalpelHan Fang, Ewa A Bergmann, Kanika Arora, et al.
Genome Research|December 5, 2006
Novel patterns of genome rearrangement and their association with survival in breast cancerJames Hicks, Alexander Krasnitz, B Lakshmi, et al.
Blood|October 17, 2008
Novel genomic alterations and clonal evolution in chronic lymphocytic leukemia revealed by representational oligonucleotide microarray analysis (ROMA)Vladimir Grubor, Alex Krasnitz, Jennifer E Troge, et al.
Pageof 8

Showing results (51-60 of 71) with videos related to

Sort By:
Pageof 8
Cell|November 18, 2008
An oncogenomics-based in vivo RNAi screen identifies tumor suppressors in liver cancerLars Zender, Wen Xue, Johannes Zuber, et al.
Human Genetics|August 28, 2013
The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart diseaseDorothy Warburton, Michael Ronemus, Jennie Kline, et al.
Communications Biology|September 2, 2021
Rates of contributory de novo mutation in high and low-risk autism familiesSeungtai Yoon, Adriana Munoz, Boris Yamrom, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 2012
A cluster of cooperating tumor-suppressor gene candidates in chromosomal deletionsWen Xue, Thomas Kitzing, Stephanie Roessler, et al.
Genome Research|September 17, 2003
Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variationRobert Lucito, John Healy, Joan Alexander, et al.
Science (New York, N.Y.)|July 27, 2004
Large-scale copy number polymorphism in the human genomeJonathan Sebat, B Lakshmi, Jennifer Troge, et al.
Genome Biology|September 27, 2025
Hybrid BAG-seq: DNA and RNA from the same single nucleus reveals interactions between genomic and transcriptomic landscapes in human tumor samplesSiran Li, Joan Alexander, Jude Kendall, et al.
Nature Protocols|November 18, 2016
Indel variant analysis of short-read sequencing data with ScalpelHan Fang, Ewa A Bergmann, Kanika Arora, et al.
Genome Research|December 5, 2006
Novel patterns of genome rearrangement and their association with survival in breast cancerJames Hicks, Alexander Krasnitz, B Lakshmi, et al.
Blood|October 17, 2008
Novel genomic alterations and clonal evolution in chronic lymphocytic leukemia revealed by representational oligonucleotide microarray analysis (ROMA)Vladimir Grubor, Alex Krasnitz, Jennifer E Troge, et al.
Pageof 8