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Michael E Zwick

Showing results (31-40 of 75) with videos related to

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BMC Bioinformatics|September 22, 2010
SeqAnt: a web service to rapidly identify and annotate DNA sequence variationsAmol Carl Shetty, Prashanth Athri, Kajari Mondal, et al.
JIMD Reports|February 15, 2015
A De Novo Variant in Galactose-1-P Uridylyltransferase (GALT) Leading to Classic GalactosemiaThanh-Thanh Claire V Tran, Ying Liu, Michael E Zwick, et al.
Open Access Bioinformatics|March 8, 2011
Microarray oligonucleotide probe designer (MOPeD): A web serviceViren C Patel, Kajari Mondal, Amol Carl Shetty, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 2017
Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizesH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2017
PEMapper and PECaller provide a simplified approach to whole-genome sequencingH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Plos One|March 12, 2010
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotypeStephen C Collins, Brad Coffee, Paul J Benke, et al.
American Journal of Epidemiology|July 9, 2020
Bayesian Pathway Analysis for Complex InteractionsJames W Baurley, Anders Kjærsgaard, Michael E Zwick, et al.
Inflammatory Bowel Diseases|March 27, 2012
Common NOD2 risk variants in African Americans with Crohn's disease are due exclusively to recent Caucasian admixtureOloruntosin Adeyanju, David T Okou, Clifton Huang, et al.
Genome Research|January 21, 2010
Copy number abnormalities in sporadic canine colorectal cancersJie Tang, Shoshona Le, Liang Sun, et al.
Genome Medicine|May 10, 2023
High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencingFeyza Yilmaz, Umamaheswaran Gurusamy, Trenell J Mosley, et al.
Pageof 8

Showing results (31-40 of 75) with videos related to

Sort By:
Pageof 8
BMC Bioinformatics|September 22, 2010
SeqAnt: a web service to rapidly identify and annotate DNA sequence variationsAmol Carl Shetty, Prashanth Athri, Kajari Mondal, et al.
JIMD Reports|February 15, 2015
A De Novo Variant in Galactose-1-P Uridylyltransferase (GALT) Leading to Classic GalactosemiaThanh-Thanh Claire V Tran, Ying Liu, Michael E Zwick, et al.
Open Access Bioinformatics|March 8, 2011
Microarray oligonucleotide probe designer (MOPeD): A web serviceViren C Patel, Kajari Mondal, Amol Carl Shetty, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 2017
Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizesH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 23, 2017
PEMapper and PECaller provide a simplified approach to whole-genome sequencingH Richard Johnston, Pankaj Chopra, Thomas S Wingo, et al.
Plos One|March 12, 2010
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotypeStephen C Collins, Brad Coffee, Paul J Benke, et al.
American Journal of Epidemiology|July 9, 2020
Bayesian Pathway Analysis for Complex InteractionsJames W Baurley, Anders Kjærsgaard, Michael E Zwick, et al.
Inflammatory Bowel Diseases|March 27, 2012
Common NOD2 risk variants in African Americans with Crohn's disease are due exclusively to recent Caucasian admixtureOloruntosin Adeyanju, David T Okou, Clifton Huang, et al.
Genome Research|January 21, 2010
Copy number abnormalities in sporadic canine colorectal cancersJie Tang, Shoshona Le, Liang Sun, et al.
Genome Medicine|May 10, 2023
High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencingFeyza Yilmaz, Umamaheswaran Gurusamy, Trenell J Mosley, et al.
Pageof 8