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Michael Ronemus

Showing results (11-20 of 22) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|December 31, 2011
Reducing system noise in copy number data using principal components of self-self hybridizationsYoon-ha Lee, Michael Ronemus, Jude Kendall, et al.
Genome Medicine|November 27, 2014
Reducing INDEL calling errors in whole genome and exome sequencing dataHan Fang, Yiyang Wu, Giuseppe Narzisi, et al.
Neuron|June 11, 2011
Rare de novo and transmitted copy-number variation in autistic spectrum disordersDan Levy, Michael Ronemus, Boris Yamrom, 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.
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.
American Journal of Human Genetics|August 7, 2012
Rare de novo germline copy-number variation in testicular cancerZsofia K Stadler, Diane Esposito, Sohela Shah, et al.
Circulation Research|September 11, 2014
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence dataJoseph T Glessner, Alexander G Bick, Kaoru Ito, et al.
Neuron|May 1, 2012
De novo gene disruptions in children on the autistic spectrumIvan Iossifov, Michael Ronemus, Dan Levy, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Proceedings of the National Academy of Sciences of the United States of America|December 31, 2011
Reducing system noise in copy number data using principal components of self-self hybridizationsYoon-ha Lee, Michael Ronemus, Jude Kendall, et al.
Genome Medicine|November 27, 2014
Reducing INDEL calling errors in whole genome and exome sequencing dataHan Fang, Yiyang Wu, Giuseppe Narzisi, et al.
Neuron|June 11, 2011
Rare de novo and transmitted copy-number variation in autistic spectrum disordersDan Levy, Michael Ronemus, Boris Yamrom, 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.
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.
American Journal of Human Genetics|August 7, 2012
Rare de novo germline copy-number variation in testicular cancerZsofia K Stadler, Diane Esposito, Sohela Shah, et al.
Circulation Research|September 11, 2014
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence dataJoseph T Glessner, Alexander G Bick, Kaoru Ito, et al.
Neuron|May 1, 2012
De novo gene disruptions in children on the autistic spectrumIvan Iossifov, Michael Ronemus, Dan Levy, et al.
Pageof 3