The next -
generation sequencing analyzes roughly 2 % of those 3 billion base pairs.
Not exact matches
The FEMTO Pulse is designed to meet the needs of next -
generation sequencing (NGS) systems
analyzing ever - longer DNA fragments.
The convergence of several factors explains the trend: cheaper genetic
sequencing technologies, the discovery of new oncogenes (genes that can cause a normal cell to become cancerous), a new
generation of computers and bioinformatics that can
analyze vast amounts of data, and a multibillion - dollar effort by researchers inside and outside the pharma industry to develop targeted drugs and companion diagnostics for cancer.
Working in tandem, Keim's Arizona team and Herman Meyer and Markus Antwerpen at the Bundeswehr Institute of Microbiology in Munich,
sequenced the strains using next -
generation sequencing (NGS), a technique that allowed them to
analyze every genetic difference at the level of single letter changes to the genetic code.
Using whole exome
sequencing (a next generation test to analyze the exons or coding regions of thousands of genes simultaneously) conducted at the Baylor College of Medicine Human Genome Sequencing Center, the researchers identified CLP1 mutations in two unrelated families with the
sequencing (a next
generation test to
analyze the exons or coding regions of thousands of genes simultaneously) conducted at the Baylor College of Medicine Human Genome
Sequencing Center, the researchers identified CLP1 mutations in two unrelated families with the
Sequencing Center, the researchers identified CLP1 mutations in two unrelated families with the disorder.
They then comprehensively
analyzed the changes in the whole genome and epigenome using next
generation deep
sequencing.
We use next -
generation sequencing to
analyze circulating and shed biomarkers in order to develop better approaches for primary, secondary, and tertiary ovarian cancer prevention.
Metagenomics: Tools and Insights for
Analyzing Next -
Generation Sequencing Data Derived from Biodiversity Studies — Anastasis Oulas — Bioinform Biol Insights — May 2015
Additional lines are being developed to
analyze next -
generation sequencing transcriptome data, and to construct and work with phylogenetic trees.
I co-led the research team that first
sequenced and
analyzed a whole cancer genome using next -
generation sequencing methods.
To characterize their viral genomes in greater depth, we
analyzed RNA extracts from these 3 samples by unbiased next -
generation, or «deep»
sequencing.
In light of these limitations, next -
generation sequencing (NGS) represents a more appropriate technique for
analyzing these type of samples, mainly due to the high resolving power that characterizes NGS platforms conjointly with bioinformatics tools.