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Blood
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September 2, 2021
The crux of Cux1 in myeloid neoplasms
Ian J Majewski
Biochemical Society Transactions
|
March 10, 2019
On fitness: how do mutations shape the biology of cancer?
Ian J Majewski
Nature Medicine
|
March 10, 2011
Taming the dragon: genomic biomarkers to individualize the treatment of cancer
Ian J Majewski, René Bernards
Bioinformatics (Oxford, England)
|
June 16, 2021
Detecting copy number alterations in RNA-Seq using SuperFreq
Christoffer Flensburg, Alicia Oshlack, Ian J Majewski
Genome Medicine
|
May 29, 2015
JAFFA: High sensitivity transcriptome-focused fusion gene detection
Nadia M Davidson, Ian J Majewski, Alicia Oshlack
Plos Computational Biology
|
February 14, 2020
SuperFreq: Integrated mutation detection and clonal tracking in cancer
Christoffer Flensburg, Tobias Sargeant, Alicia Oshlack, et al.
Nucleic Acids Research
|
November 12, 2023
Uridine-cytidine kinase 2 potentiates the mutagenic influence of the antiviral β-d-N4-hydroxycytidine
Zhen Xu, Christoffer Flensburg, Rebecca A Bilardi, et al.
BMC Bioinformatics
|
December 2, 2020
Finding a suitable library size to call variants in RNA-Seq
Anna Quaglieri, Christoffer Flensburg, Terence P Speed, et al.
The Annals of Applied Statistics
|
April 4, 2017
ROBUST HYPERPARAMETER ESTIMATION PROTECTS AGAINST HYPERVARIABLE GENES AND IMPROVES POWER TO DETECT DIFFERENTIAL EXPRESSION
Belinda Phipson, Stanley Lee, Ian J Majewski, et al.
Genome Biology
|
October 23, 2021
MINTIE: identifying novel structural and splice variants in transcriptomes using RNA-seq data
Marek Cmero, Breon Schmidt, Ian J Majewski, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 46) with videos related to
Sort By:
Page
of 5
Blood
|
September 2, 2021
The crux of Cux1 in myeloid neoplasms
Ian J Majewski
Biochemical Society Transactions
|
March 10, 2019
On fitness: how do mutations shape the biology of cancer?
Ian J Majewski
Nature Medicine
|
March 10, 2011
Taming the dragon: genomic biomarkers to individualize the treatment of cancer
Ian J Majewski, René Bernards
Bioinformatics (Oxford, England)
|
June 16, 2021
Detecting copy number alterations in RNA-Seq using SuperFreq
Christoffer Flensburg, Alicia Oshlack, Ian J Majewski
Genome Medicine
|
May 29, 2015
JAFFA: High sensitivity transcriptome-focused fusion gene detection
Nadia M Davidson, Ian J Majewski, Alicia Oshlack
Plos Computational Biology
|
February 14, 2020
SuperFreq: Integrated mutation detection and clonal tracking in cancer
Christoffer Flensburg, Tobias Sargeant, Alicia Oshlack, et al.
Nucleic Acids Research
|
November 12, 2023
Uridine-cytidine kinase 2 potentiates the mutagenic influence of the antiviral β-d-N4-hydroxycytidine
Zhen Xu, Christoffer Flensburg, Rebecca A Bilardi, et al.
BMC Bioinformatics
|
December 2, 2020
Finding a suitable library size to call variants in RNA-Seq
Anna Quaglieri, Christoffer Flensburg, Terence P Speed, et al.
The Annals of Applied Statistics
|
April 4, 2017
ROBUST HYPERPARAMETER ESTIMATION PROTECTS AGAINST HYPERVARIABLE GENES AND IMPROVES POWER TO DETECT DIFFERENTIAL EXPRESSION
Belinda Phipson, Stanley Lee, Ian J Majewski, et al.
Genome Biology
|
October 23, 2021
MINTIE: identifying novel structural and splice variants in transcriptomes using RNA-seq data
Marek Cmero, Breon Schmidt, Ian J Majewski, et al.
Page
of 5