Cancer Sequencing

Several sequencing approaches are employed to understand and examine tumor development and progression. These include whole genome as well as RNA sequencing. Here is the latest research on cancer sequencing.

October 21, 2020

Detection of ERBB2 amplification in uterine serous carcinoma by next-generation sequencing: an approach highly concordant with standard assays

Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
Carrie L RobinsonDavid L Kolin
October 19, 2020
Open Access

Comparison of variant allele frequency and number of mutant molecules as units of measurement for circulating tumor DNA

Molecular Oncology
Manouk K BosJohn W M Martens
October 27, 2020
Open Access

Fractionated small cell-free DNA increases possibility to detect cancer-related gene mutations in advanced colorectal cancer

JGH Open : an Open Access Journal of Gastroenterology and Hepatology
Yasuaki IshidaNobuyuki Enomoto
October 22, 2020
Open Access

Identification of fetal unmodified and 5-hydroxymethylated CG sites in maternal cell-free DNA for non-invasive prenatal testing

Clinical Epigenetics
Juozas GordevičiusEdita Kriukienė
October 14, 2020
Open Access

Landscape of FGF /FGFR Alterations in 12,372 Chinese Cancer Patients

Journal of Cancer
Wei ZuoYongmei Yin
October 13, 2020
Review
Open Access

HPV Detection in Head and Neck Squamous Cell Carcinomas: What Is the Issue?

Frontiers in Oncology
Jeremy Gbenakpon AugustinCécile Badoual
October 18, 2020
Open Access

BRCA1 and BRCA2 genes mutations among high risk breast cancer patients in Jordan

Scientific Reports
Munir Abu-HelalahAbdalla Awidi
October 22, 2020

Genomic aberrations and late recurrence in postmenopausal women with hormone receptor-positive early breast cancer: Results from the SOLE Trial

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
Elena Guerini-RoccoMarco Colleoni

Sign up to follow this feed and discover related papers.

Related Feeds

Alignment-free Sequence Analysis Tools

Alignment-free sequence analyses have been applied to problems ranging from whole-genome phylogeny to the classification of protein families, identification of horizontally transferred genes, and detection of recombined sequences. Here is the latest research.

Alzheimer's Disease: RNA Sequencing

RNA sequencing is used to reveal the presence and quantity of RNA in a given sample. In this feed, RNA sequencing investigates the genetic and molecular mechanisms related to the pathophysiology of Alzheimer's disease (AD). Here are the latest discoveries pertaining to RNA sequencing and this disease.

Applications of Molecular Barcoding

The concept of molecular barcoding is that each original DNA or RNA molecule is attached to a unique sequence barcode. Sequence reads having different barcodes represent different original molecules, while sequence reads having the same barcode are results of PCR duplication from one original molecule. Discover the latest research on molecular barcoding here.

Bioconductor Software Package: Human Cell Atlas

The open source software R / Bioconductor is used for statistical analysis and visualization, with continual generation of new analysis packages and updates. Find the latest research on Programming: Bioconductor Software Packages here.

Bioconductor software package (programming)

The open source software R / Bioconductor is used for statistical analysis and visualization, with continual generation of new analysis packages and updates. Find the latest research on programming and Bioconductor here.

Bioinformatics in Biomedicine

Bioinformatics in biomedicine incorporates computer science, biology, chemistry, medicine, mathematics and statistics. Discover the latest research on bioinformatics in biomedicine here.

CRISPR & Single Cell Analyses

CRISPR-Cas system enables the editing of genes to create or correct mutations. This feed focuses on CRISPR-Cas applications relevant to single cell analyses. Here is the latest research.

CRISPR (general)

Clustered regularly interspaced short palindromic repeats (CRISPR) are DNA sequences in the genome that are recognized and cleaved by CRISPR-associated proteins (Cas). CRISPR-Cas system enables the editing of genes to create or correct mutations. Discover the latest research on CRISPR here.

CRISPR for Genome Editing

Genome editing technologies enable the editing of genes to create or correct mutations. Clustered regularly interspaced short palindromic repeats (CRISPR) are DNA sequences in the genome that are recognized and cleaved by CRISPR-associated proteins (Cas). Here is the latest research on the use of CRISPR-Cas system in gene editing.

Cancer Epigenetics

Epigenetic changes are present and dysregulated in many cancers, including DNA methylation, non-coding RNA segments and post-translational protein modifications. The epigenetic changes may or may not provide advantages for the cancer cells. Here is the latest research on cancer epigenetics.

© 2020 Meta ULC. All rights reserved
/feed-previews/cancer-sequencing/a7561921-ef74-4eb4-ba5e-3cb5c294a4c8