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BMC Genomics
|
November 3, 2005
SNiPer: improved SNP genotype calling for Affymetrix 10K GeneChip microarray data
Matthew J Huentelman, David W Craig, Albert D Shieh, et al.
Nucleic Acids Research
|
November 10, 2011
PINA v2.0: mining interactome modules
Mark J Cowley, Mark Pinese, Karin S Kassahn, et al.
Gigascience
|
April 4, 2026
Cancer genome standards for long-read sequencing using cancer cell line mixtures
Jia Zhang, Ho Yi Wong, Lingchen Liu, et al.
Journal of Proteome Research
|
March 12, 2015
PGTools: A Software Suite for Proteogenomic Data Analysis and Visualization
Shivashankar H Nagaraj, Nicola Waddell, Anil K Madugundu, et al.
Plos Genetics
|
September 5, 2008
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays
Nils Homer, Szabolcs Szelinger, Margot Redman, et al.
Human Mutation
|
September 12, 2022
Analysis of hereditary cancer gene variant classifications from ClinVar indicates a need for regular reassessment of clinical assertions
Aimee L Davidson, Olga Kondrashova, Conrad Leonard, et al.
Human Mutation
|
February 18, 2021
Considerations for using population frequency data in germline variant interpretation: Cancer syndrome genes as a model
Aimee L Davidson, Conrad Leonard, Lambros T Koufariotis, et al.
Pigment Cell & Melanoma Research
|
December 27, 2016
Mutation load in melanoma is affected by MC1R genotype
Peter A Johansson, Antonia L Pritchard, Ann-Marie Patch, et al.
Cancers
|
April 30, 2021
Tumor Signature Analysis Implicates Hereditary Cancer Genes in Endometrial Cancer Development
Olga Kondrashova, Jannah Shamsani, Tracy A O'Mara, et al.
Neuro-Oncology
|
February 9, 2023
Efficient detection and monitoring of pediatric brain malignancies with liquid biopsy based on patient-specific somatic mutation screening
Marija Kojic, Mellissa K Maybury, Nicola Waddell, et al.
Page
of 22
Search research articles
Search
Showing results (111-120 of 219) with videos related to
Sort By:
Page
of 22
BMC Genomics
|
November 3, 2005
SNiPer: improved SNP genotype calling for Affymetrix 10K GeneChip microarray data
Matthew J Huentelman, David W Craig, Albert D Shieh, et al.
Nucleic Acids Research
|
November 10, 2011
PINA v2.0: mining interactome modules
Mark J Cowley, Mark Pinese, Karin S Kassahn, et al.
Gigascience
|
April 4, 2026
Cancer genome standards for long-read sequencing using cancer cell line mixtures
Jia Zhang, Ho Yi Wong, Lingchen Liu, et al.
Journal of Proteome Research
|
March 12, 2015
PGTools: A Software Suite for Proteogenomic Data Analysis and Visualization
Shivashankar H Nagaraj, Nicola Waddell, Anil K Madugundu, et al.
Plos Genetics
|
September 5, 2008
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays
Nils Homer, Szabolcs Szelinger, Margot Redman, et al.
Human Mutation
|
September 12, 2022
Analysis of hereditary cancer gene variant classifications from ClinVar indicates a need for regular reassessment of clinical assertions
Aimee L Davidson, Olga Kondrashova, Conrad Leonard, et al.
Human Mutation
|
February 18, 2021
Considerations for using population frequency data in germline variant interpretation: Cancer syndrome genes as a model
Aimee L Davidson, Conrad Leonard, Lambros T Koufariotis, et al.
Pigment Cell & Melanoma Research
|
December 27, 2016
Mutation load in melanoma is affected by MC1R genotype
Peter A Johansson, Antonia L Pritchard, Ann-Marie Patch, et al.
Cancers
|
April 30, 2021
Tumor Signature Analysis Implicates Hereditary Cancer Genes in Endometrial Cancer Development
Olga Kondrashova, Jannah Shamsani, Tracy A O'Mara, et al.
Neuro-Oncology
|
February 9, 2023
Efficient detection and monitoring of pediatric brain malignancies with liquid biopsy based on patient-specific somatic mutation screening
Marija Kojic, Mellissa K Maybury, Nicola Waddell, et al.
Page
of 22