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Melanie Bahlo

Showing results (1-10 of 280) with videos related to

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The Medical Journal of Australia|June 3, 2023
Young-onset dementia diagnosis, management and careMelanie Bahlo
Genetic Epidemiology|August 6, 2011
X chromosome association testing in genome wide association studiesPeter F Hickey, Melanie Bahlo
Bioinformatics (Oxford, England)|May 7, 2016
XIBD: software for inferring pairwise identity by descent on the X chromosomeLyndal Henden, David Wakeham, Melanie Bahlo
Annual Review of Genomics and Human Genetics|April 28, 2020
The Genetics of EpilepsyPiero Perucca, Melanie Bahlo, Samuel F Berkovic
BMC Medical Genomics|June 18, 2015
High-resolution characterization of sequence signatures due to non-random cleavage of cell-free DNADineika Chandrananda, Natalie P Thorne, Melanie Bahlo
F1000Research|November 25, 2024
AmpSeqR: an R package for amplicon deep sequencing data analysisJiru Han, Jacob E Munro, Melanie Bahlo
Emerging Topics in Life Sciences|September 21, 2023
Detection and discovery of repeat expansions in ataxia enabled by next-generation sequencing: present and futureHaloom Rafehi, Mark F Bennett, Melanie Bahlo
Communications Biology|February 19, 2025
TBtypeR: Sensitive detection and sublineage classification of Mycobacterium tuberculosis complex mixed-strain infectionsJacob E Munro, Anna K Coussens, Melanie Bahlo
Genetics|June 1, 2014
Dating rare mutations from small samples with dense marker dataLuke C Gandolfo, Melanie Bahlo, Terence P Speed
Bioinformatics Advances|April 22, 2025
GeneSetPheno: a web application for the integration, summary, and visualization of gene and variant-phenotype associations across gene setsJiru Han, Zachary F Gerring, Longfei Wang, et al.
Pageof 28

Showing results (1-10 of 280) with videos related to

Sort By:
Pageof 28
The Medical Journal of Australia|June 3, 2023
Young-onset dementia diagnosis, management and careMelanie Bahlo
Genetic Epidemiology|August 6, 2011
X chromosome association testing in genome wide association studiesPeter F Hickey, Melanie Bahlo
Bioinformatics (Oxford, England)|May 7, 2016
XIBD: software for inferring pairwise identity by descent on the X chromosomeLyndal Henden, David Wakeham, Melanie Bahlo
Annual Review of Genomics and Human Genetics|April 28, 2020
The Genetics of EpilepsyPiero Perucca, Melanie Bahlo, Samuel F Berkovic
BMC Medical Genomics|June 18, 2015
High-resolution characterization of sequence signatures due to non-random cleavage of cell-free DNADineika Chandrananda, Natalie P Thorne, Melanie Bahlo
F1000Research|November 25, 2024
AmpSeqR: an R package for amplicon deep sequencing data analysisJiru Han, Jacob E Munro, Melanie Bahlo
Emerging Topics in Life Sciences|September 21, 2023
Detection and discovery of repeat expansions in ataxia enabled by next-generation sequencing: present and futureHaloom Rafehi, Mark F Bennett, Melanie Bahlo
Communications Biology|February 19, 2025
TBtypeR: Sensitive detection and sublineage classification of Mycobacterium tuberculosis complex mixed-strain infectionsJacob E Munro, Anna K Coussens, Melanie Bahlo
Genetics|June 1, 2014
Dating rare mutations from small samples with dense marker dataLuke C Gandolfo, Melanie Bahlo, Terence P Speed
Bioinformatics Advances|April 22, 2025
GeneSetPheno: a web application for the integration, summary, and visualization of gene and variant-phenotype associations across gene setsJiru Han, Zachary F Gerring, Longfei Wang, et al.
Pageof 28