Human Genome Sequencing centerBaylor college of Medicine Company Profile

00:19 EDT 20th March 2018 | BioPortfolio



One Baylor plaza,MSC-226
United States of America


Phone: 713.798.6539
Fax: 713.798.5741

News Articles [2766 Associated News Articles listed on BioPortfolio]

Update: Pocket Device makes its Debut in Whole Human Genome Sequencing

Update (30/1/18): Oxford Nanopore has published a study in Nature Biotechnology outlining the first use of its pocket MinION device to sequence a human genome. The biotech’s device was able to ...

Whole-Genome Sequencing of the World’s Oldest People

December 2014 Whole-Genome Sequencing of the World’s Oldest People A group of scientists have performed whole-genome sequencing on 17 of the world’s 74 remaining supercentenarians (110 y...

Precision Medicine, Genome Sequencing, and Improved Population Health

This Viewpoint summarizes a 2017 NASEM Roundtable on Genomics and Precision Health that shared experiences of US health systems with use of genome sequencing for clinical and research applications and...

A New Day? Fast, Cheap Human Genome Sequencing Will Open Doors

Researchers sequenced the human genome using handheld sequencers in just a few weeks, opening the door to new clinical applications, experts say. Medscape Medical News

Oxford Nanopore's tech reaches genome sequencing landmark

A  new technique for gene sequencing has produced the most complete human genome ever assembled with a single technology - the nanapore, developed by UK company Oxford Nanopore Technologies. The m...

Complexity of computational analysis of genome sequencing and reporting

Dean Pavlick presents at ecancer's Milan Summit on Precision Medicine 2018 about the complexity of computational analysis or genome sequencing and reporting. He discusses genomic alterations and trea...

Research signals arrival of a complete human genome

Research have just published attempts to close huge gaps remain in our genomic reference map. The research uses nanopore long-read sequencing to generate the first complete and accurate linear map of ...

Rapid whole-genome sequencing of neonatal ICU patients is useful and cost-effective

(American Society of Human Genetics) Rapid whole-genome sequencing of acutely ill neonatal intensive care unit (NICU) patients in the first few days of life yields clinically useful diagnoses in many ...

PubMed Articles [6648 Associated PubMed Articles listed on BioPortfolio]

A primer to clinical genome sequencing.

Genome sequencing is now available as a clinical diagnostic test. There is a significant knowledge and translation gap for nongenetic specialists of the processes necessary to generate and interpret c...

Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers.

PurposeAs massively parallel sequencing is increasingly being used for clinical decision making, it has become critical to understand parameters that affect sequencing quality and to establish methods...

CORRIGENDUM: What are people willing to pay for whole-genome sequencing information, and who decides what they receive?

This corrects the article DOI: 10.1038/gim.2016.61.

DNA sequencing at 40: past, present and future.

This review commemorates the 40th anniversary of DNA sequencing, a period in which we have already witnessed multiple technological revolutions and a growth in scale from a few kilobases to the first ...

Controversy and Debate on Clinical Genomics Sequencing - Paper 2: Clinical Genome-Wide Sequencing: Don't Throw Out the Baby With The Bathwater!

Genome-wide (exome or whole genome) sequencing with appropriate genetic counselling should be considered for any patient with a suspected mendelian disease that has not been identified by conventional...

Clinical Trials [4242 Associated Clinical Trials listed on BioPortfolio]

Diagnostic Odyssey: Whole Genome Sequencing (WGS)

The goal of this collaborative research is to study human genomes in children with suspected congenital disease, multiple-congenital anomalies and/or multi-organ disease of unknown etiolog...

Whole Genome Sequencing in the Detection of Rare Undiagnosed Genetic Diseases in Children in China

To assess the indications and diagnostic efficiency of whole genome sequencing (WGS) in pediatric patients with unexplained intellectual disability/developmental delay, multiple congenital...

The VetSeq Study: a Pilot Study of Genome Sequencing in Veteran Care

The VetSeq Study is a pilot intervention study exploring the feasibility of integrating genome sequencing into clinical care at the VA Boston Healthcare System.

Rapid Whole Genome Sequencing Study

Rapid Whole Genome Sequencing (rWGS) has proven to provide much faster diagnoses than traditional clinical testing, including clinical Whole Exome Sequencing (WES) and standard Whole Genom...

Genomic Sequencing in Acutely Ill Neonates

The purpose of this study is to compare the effectiveness of rapid next generation sequencing (NGS, such as whole genome sequencing1) with current practice to provide diagnostic or prognos...

Companies [2585 Associated Companies listed on BioPortfolio]

Human Genome Sequencing centerBaylor college of Medicine


Complete Genomics Inc.

Founded in 2006, Complete Genomics is a California company that has developed a novel approach to sequencing human DNA. Complete Genomics combines its proprietary third-generation...

Nucleics Pty Ltd

Nucleics was founded in 1999 by Dr Paul March and Dr Daniel Tillett to develop the ASIN genome sequencing technology. Nucleics is focused on the development of automated DNA sequencing services, reage...

Longenity Inc

Longenity Inc. is a biotechnology company using genomics, bioinformatics, and systems biology, founded for the purpose of understanding normal aging, and common pathologies of human aging. Longenity ...

Genome News Network

Genomics is News. It is often hyped. It can be difficult to understand. Sometimes it raises more questions than it can yet answer. But its importance to biology and medicine cannot be overstated; nor ...

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