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Plos Computational Biology
|
September 5, 2014
A probabilistic model to predict clinical phenotypic traits from genome sequencing
Yun-Ching Chen, Christopher Douville, Cheng Wang, et al.
Plos One
|
May 31, 2018
Integration of genetic and metabolic features related to sialic acid metabolism distinguishes human breast cell subtypes
Christopher T Saeui, Alison V Nairn, Melina Galizzi, et al.
Human Mutation
|
July 29, 2014
Experimental assessment of splicing variants using expression minigenes and comparison with in silico predictions
Neeraj Sharma, Patrick R Sosnay, Anabela S Ramalho, et al.
Elife
|
March 4, 2022
Detection of malignant peripheral nerve sheath tumors in patients with neurofibromatosis using aneuploidy and mutation identification in plasma
Austin K Mattox, Christopher Douville, Natalie Silliman, et al.
Cancer Prevention Research (Philadelphia, Pa.)
|
January 31, 2015
Cleaved NOTCH1 Expression Pattern in Head and Neck Squamous Cell Carcinoma Is Associated with NOTCH1 Mutation, HPV Status, and High-Risk Features
Eleni M Rettig, Christine H Chung, Justin A Bishop, et al.
Cancer Genetics
|
April 18, 2025
Analytical validation of the Belay Vantage™ assay for evaluation of MGMT promoter methylation using enzymatically converted tumorDNA from cerebrospinal fluid
Kala F Schilter, Qian Nie, Jennifer N Adams, et al.
Nature Biotechnology
|
May 4, 2021
Detection of low-frequency DNA variants by targeted sequencing of the Watson and Crick strands
Joshua D Cohen, Christopher Douville, Jonathan C Dudley, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 4, 2023
Aneuploidy Landscape in Precursors of Ovarian Cancer
Yeh Wang, Christopher Douville, Yen-Wei Chien, et al.
Cancers
|
May 4, 2026
Clinical Validation of the Belay Ascent™ Test to Report on Chromosomal Arm-Level Aneuploidy and Gene-Level Copy Number Variants in Cerebrospinal Fluid Using Low-Pass Whole-Genome Sequencing
Qian Nie, Kala F Schilter, Alexandra Larson, et al.
Plos Computational Biology
|
September 16, 2021
Eliminating accidental deviations to minimize generalization error and maximize replicability: Applications in connectomics and genomics
Eric W Bridgeford, Shangsi Wang, Zeyi Wang, et al.
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Showing results (11-20 of 55) with videos related to
Sort By:
Page
of 6
Plos Computational Biology
|
September 5, 2014
A probabilistic model to predict clinical phenotypic traits from genome sequencing
Yun-Ching Chen, Christopher Douville, Cheng Wang, et al.
Plos One
|
May 31, 2018
Integration of genetic and metabolic features related to sialic acid metabolism distinguishes human breast cell subtypes
Christopher T Saeui, Alison V Nairn, Melina Galizzi, et al.
Human Mutation
|
July 29, 2014
Experimental assessment of splicing variants using expression minigenes and comparison with in silico predictions
Neeraj Sharma, Patrick R Sosnay, Anabela S Ramalho, et al.
Elife
|
March 4, 2022
Detection of malignant peripheral nerve sheath tumors in patients with neurofibromatosis using aneuploidy and mutation identification in plasma
Austin K Mattox, Christopher Douville, Natalie Silliman, et al.
Cancer Prevention Research (Philadelphia, Pa.)
|
January 31, 2015
Cleaved NOTCH1 Expression Pattern in Head and Neck Squamous Cell Carcinoma Is Associated with NOTCH1 Mutation, HPV Status, and High-Risk Features
Eleni M Rettig, Christine H Chung, Justin A Bishop, et al.
Cancer Genetics
|
April 18, 2025
Analytical validation of the Belay Vantage™ assay for evaluation of MGMT promoter methylation using enzymatically converted tumorDNA from cerebrospinal fluid
Kala F Schilter, Qian Nie, Jennifer N Adams, et al.
Nature Biotechnology
|
May 4, 2021
Detection of low-frequency DNA variants by targeted sequencing of the Watson and Crick strands
Joshua D Cohen, Christopher Douville, Jonathan C Dudley, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 4, 2023
Aneuploidy Landscape in Precursors of Ovarian Cancer
Yeh Wang, Christopher Douville, Yen-Wei Chien, et al.
Cancers
|
May 4, 2026
Clinical Validation of the Belay Ascent™ Test to Report on Chromosomal Arm-Level Aneuploidy and Gene-Level Copy Number Variants in Cerebrospinal Fluid Using Low-Pass Whole-Genome Sequencing
Qian Nie, Kala F Schilter, Alexandra Larson, et al.
Plos Computational Biology
|
September 16, 2021
Eliminating accidental deviations to minimize generalization error and maximize replicability: Applications in connectomics and genomics
Eric W Bridgeford, Shangsi Wang, Zeyi Wang, et al.
Page
of 6