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Frontiers in Medicine
|
April 25, 2022
Bioinformatic Challenges Detecting Genetic Variation in Precision Medicine Programs
Matt A Field
Immunology and Cell Biology
|
July 6, 2020
Detecting pathogenic variants in autoimmune diseases using high-throughput sequencing
Matt A Field
Peerj
|
July 28, 2021
Efficacy of computational predictions of the functional effect of idiosyncratic pharmacogenetic variants
Hannah McConnell, T Daniel Andrews, Matt A Field
Methods in Molecular Biology (Clifton, N.J.)
|
February 19, 2021
Detecting Causal Variants in Mendelian Disorders Using Whole-Genome Sequencing
Abdul Rezzak Hamzeh, T Daniel Andrews, Matt A Field
Briefings in Bioinformatics
|
June 8, 2025
TARGET-SL: precision essential gene prediction using driver prioritisation and synthetic lethality
Rhys Gillman, Matt A Field, Ulf Schmitz, et al.
Briefings in Bioinformatics
|
December 11, 2025
Bioinformatics frameworks for single-cell long-read sequencing: unlocking isoform-level resolution
Saloni Bhatia, Matt A Field, Lionel Hebbard, et al.
Human Genomics
|
August 23, 2025
Increasing pathogenic germline variant diagnosis rates in precision medicine: current best practices and future opportunities
Sonam Dukda, Manoharan Kumar, Andrew Calcino, et al.
Computational and Structural Biotechnology Journal
|
October 23, 2023
Identifying cancer driver genes in individual tumours
Rhys Gillman, Matt A Field, Ulf Schmitz, et al.
Molecular Ecology
|
May 9, 2025
Putting Structural Variants Into Practice: The Role of Chromosomal Inversions in the Management of Marine Environments
Nadja M Schneller, Jan M Strugnell, Matt A Field, et al.
Animal Models and Experimental Medicine
|
February 27, 2026
Molecular characterization of the A52 murine hepatocellular carcinoma cell line
Rhys Gillman, Eun Jin Sun, Miriam Wankell, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 45) with videos related to
Sort By:
Page
of 5
Frontiers in Medicine
|
April 25, 2022
Bioinformatic Challenges Detecting Genetic Variation in Precision Medicine Programs
Matt A Field
Immunology and Cell Biology
|
July 6, 2020
Detecting pathogenic variants in autoimmune diseases using high-throughput sequencing
Matt A Field
Peerj
|
July 28, 2021
Efficacy of computational predictions of the functional effect of idiosyncratic pharmacogenetic variants
Hannah McConnell, T Daniel Andrews, Matt A Field
Methods in Molecular Biology (Clifton, N.J.)
|
February 19, 2021
Detecting Causal Variants in Mendelian Disorders Using Whole-Genome Sequencing
Abdul Rezzak Hamzeh, T Daniel Andrews, Matt A Field
Briefings in Bioinformatics
|
June 8, 2025
TARGET-SL: precision essential gene prediction using driver prioritisation and synthetic lethality
Rhys Gillman, Matt A Field, Ulf Schmitz, et al.
Briefings in Bioinformatics
|
December 11, 2025
Bioinformatics frameworks for single-cell long-read sequencing: unlocking isoform-level resolution
Saloni Bhatia, Matt A Field, Lionel Hebbard, et al.
Human Genomics
|
August 23, 2025
Increasing pathogenic germline variant diagnosis rates in precision medicine: current best practices and future opportunities
Sonam Dukda, Manoharan Kumar, Andrew Calcino, et al.
Computational and Structural Biotechnology Journal
|
October 23, 2023
Identifying cancer driver genes in individual tumours
Rhys Gillman, Matt A Field, Ulf Schmitz, et al.
Molecular Ecology
|
May 9, 2025
Putting Structural Variants Into Practice: The Role of Chromosomal Inversions in the Management of Marine Environments
Nadja M Schneller, Jan M Strugnell, Matt A Field, et al.
Animal Models and Experimental Medicine
|
February 27, 2026
Molecular characterization of the A52 murine hepatocellular carcinoma cell line
Rhys Gillman, Eun Jin Sun, Miriam Wankell, et al.
Page
of 5