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Genome Medicine
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April 26, 2017
PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories
Kenneth D Doig, Andrew Fellowes, Anthony H Bell, et al.
Arxiv
|
March 31, 2025
Learning and teaching biological data science in the Bioconductor community
Jenny Drnevich, Frederick J Tan, Fabricio Almeida-Silva, et al.
Breast Cancer Research : BCR
|
August 19, 2015
Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls
Ella R Thompson, Kylie L Gorringe, Simone M Rowley, et al.
Plos Genetics
|
October 3, 2012
Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles
Ella R Thompson, Maria A Doyle, Georgina L Ryland, et al.
Plos Computational Biology
|
April 22, 2025
Learning and teaching biological data science in the Bioconductor community
Jenny Drnevich, Frederick J Tan, Fabricio Almeida-Silva, et al.
Oncotarget
|
October 28, 2015
Molecular profiling of low grade serous ovarian tumours identifies novel candidate driver genes
Sally M Hunter, Michael S Anglesio, Georgina L Ryland, et al.
Plos One
|
April 23, 2014
Bioinformatics pipelines for targeted resequencing and whole-exome sequencing of human and mouse genomes: a virtual appliance approach for instant deployment
Jason Li, Maria A Doyle, Isaam Saeed, et al.
Cancer Cell
|
July 5, 2016
Id2 and E Proteins Orchestrate the Initiation and Maintenance of MLL-Rearranged Acute Myeloid Leukemia
Margherita Ghisi, Lev Kats, Frederick Masson, et al.
Gigascience
|
October 20, 2020
A single-cell RNA-sequencing training and analysis suite using the Galaxy framework
Mehmet Tekman, Bérénice Batut, Alexander Ostrovsky, et al.
Nature Methods
|
March 30, 2021
User-friendly, scalable tools and workflows for single-cell RNA-seq analysis
Pablo Moreno, Ni Huang, Jonathan R Manning, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 39) with videos related to
Sort By:
Page
of 4
Genome Medicine
|
April 26, 2017
PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories
Kenneth D Doig, Andrew Fellowes, Anthony H Bell, et al.
Arxiv
|
March 31, 2025
Learning and teaching biological data science in the Bioconductor community
Jenny Drnevich, Frederick J Tan, Fabricio Almeida-Silva, et al.
Breast Cancer Research : BCR
|
August 19, 2015
Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls
Ella R Thompson, Kylie L Gorringe, Simone M Rowley, et al.
Plos Genetics
|
October 3, 2012
Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles
Ella R Thompson, Maria A Doyle, Georgina L Ryland, et al.
Plos Computational Biology
|
April 22, 2025
Learning and teaching biological data science in the Bioconductor community
Jenny Drnevich, Frederick J Tan, Fabricio Almeida-Silva, et al.
Oncotarget
|
October 28, 2015
Molecular profiling of low grade serous ovarian tumours identifies novel candidate driver genes
Sally M Hunter, Michael S Anglesio, Georgina L Ryland, et al.
Plos One
|
April 23, 2014
Bioinformatics pipelines for targeted resequencing and whole-exome sequencing of human and mouse genomes: a virtual appliance approach for instant deployment
Jason Li, Maria A Doyle, Isaam Saeed, et al.
Cancer Cell
|
July 5, 2016
Id2 and E Proteins Orchestrate the Initiation and Maintenance of MLL-Rearranged Acute Myeloid Leukemia
Margherita Ghisi, Lev Kats, Frederick Masson, et al.
Gigascience
|
October 20, 2020
A single-cell RNA-sequencing training and analysis suite using the Galaxy framework
Mehmet Tekman, Bérénice Batut, Alexander Ostrovsky, et al.
Nature Methods
|
March 30, 2021
User-friendly, scalable tools and workflows for single-cell RNA-seq analysis
Pablo Moreno, Ni Huang, Jonathan R Manning, et al.
Page
of 4