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J Probst

Showing results (251-260 of 283) with videos related to

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Nature Microbiology|January 31, 2018
Differential depth distribution of microbial function and putative symbionts through sediment-hosted aquifers in the deep terrestrial subsurfaceAlexander J Probst, Bethany Ladd, Jessica K Jarett, et al.
Nature Microbiology|September 19, 2022
SeqCode: a nomenclatural code for prokaryotes described from sequence dataBrian P Hedlund, Maria Chuvochina, Philip Hugenholtz, et al.
Molecular Ecology Resources|November 23, 2023
MuDoGeR: Multi-Domain Genome recovery from metagenomes made easyUlisses Rocha, Jonas Coelho Kasmanas, René Kallies, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysisSirisha Peddibhotla, Mohamed Khalifa, Frank J Probst, et al.
Genomics|November 24, 1999
Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2Y Liang, A Wang, I A Belyantseva, et al.
Nature Microbiology|August 31, 2016
A new view of the tree of lifeLaura A Hug, Brett J Baker, Karthik Anantharaman, et al.
BMC Medical Genetics|December 5, 2014
Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatelliteAvinash V Dharmadhikari, Tomasz Gambin, Przemyslaw Szafranski, et al.
Human Mutation|May 28, 2010
Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?Przemyslaw Szafranski, Christian P Schaaf, Richard E Person, et al.
F1000Research|September 30, 2024
NCBench: providing an open, reproducible, transparent, adaptable, and continuous benchmark approach for DNA-sequencing-based variant callingFriederike Hanssen, Gisela Gabernet, Famke Bäuerle, et al.
European Journal of Human Genetics : EJHG|May 23, 2013
Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testingJoanna Wiszniewska, Weimin Bi, Chad Shaw, et al.
Pageof 29

Showing results (251-260 of 283) with videos related to

Sort By:
Pageof 29
Nature Microbiology|January 31, 2018
Differential depth distribution of microbial function and putative symbionts through sediment-hosted aquifers in the deep terrestrial subsurfaceAlexander J Probst, Bethany Ladd, Jessica K Jarett, et al.
Nature Microbiology|September 19, 2022
SeqCode: a nomenclatural code for prokaryotes described from sequence dataBrian P Hedlund, Maria Chuvochina, Philip Hugenholtz, et al.
Molecular Ecology Resources|November 23, 2023
MuDoGeR: Multi-Domain Genome recovery from metagenomes made easyUlisses Rocha, Jonas Coelho Kasmanas, René Kallies, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Expanding the genotype-phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysisSirisha Peddibhotla, Mohamed Khalifa, Frank J Probst, et al.
Genomics|November 24, 1999
Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2Y Liang, A Wang, I A Belyantseva, et al.
Nature Microbiology|August 31, 2016
A new view of the tree of lifeLaura A Hug, Brett J Baker, Karthik Anantharaman, et al.
BMC Medical Genetics|December 5, 2014
Molecular and clinical analyses of 16q24.1 duplications involving FOXF1 identify an evolutionarily unstable large minisatelliteAvinash V Dharmadhikari, Tomasz Gambin, Przemyslaw Szafranski, et al.
Human Mutation|May 28, 2010
Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?Przemyslaw Szafranski, Christian P Schaaf, Richard E Person, et al.
F1000Research|September 30, 2024
NCBench: providing an open, reproducible, transparent, adaptable, and continuous benchmark approach for DNA-sequencing-based variant callingFriederike Hanssen, Gisela Gabernet, Famke Bäuerle, et al.
European Journal of Human Genetics : EJHG|May 23, 2013
Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testingJoanna Wiszniewska, Weimin Bi, Chad Shaw, et al.
Pageof 29