Genome Sequencing News
Scientists assemble Zika virus mosquito genome from scratch Mar 23, 2017 A multi-institutional team has developed a new way to sequence genomes, which can assemble the genome of an organism, entirely from scratch, dramatically cheaper and faster.
Baylor’s Human Genome Sequencing Center looks to bring adult whole genome sequencing to clinical space with unprecedented NHLBI grant Mar 1, 2017 The Human Genome Sequencing Center has been named a participant in a half-billion dollar program to bring whole genome sequencing to the forefront of clinical research.
$3.3M effort to map human genome’s intricate folding pattern Feb 2, 2017 The NIH announced eight mapping centers, including one at Baylor, will help lead the next four-year phase of its project to identify all of the functional elements contained in the human genome.
Familial test helps detect genes that cause complex diseases Jan 5, 2017 Researchers have developed a family-based association test that improves the detection in families of rare disease-causing variants of genes involved in complex conditions such as Alzheimer’s.
Baylor Genetics launches PreSeek™ - 1st non-invasive prenatal multi-gene sequencing screen Jan 4, 2017 Baylor Genetics' PreSeek allows patients a more complete picture of the risk of their pregnancy being affected by a genetic disorder.
Genes Nardilysin and OGDHL linked to human neurological conditions Dec 22, 2016 An international team of scientists has discovered that the gene, OGDHL, a key protein required for normal function of the mitochondria and its chaperone, nardilysin are linked to progressive loss of neurological function in humans.
Genetic cause identified for previously unrecognized developmental disorder Dec 22, 2016 Baylor scientists are part of an international team that has identified variants of the gene EBF3, which causes a developmental disorder with features in common with autism.
New synthetic protein captures DNA events leading to cancer, opens possibilities for improved cancer therapies Nov 18, 2016 Researchers identify opportunities for developing new drugs to neutralize molecular intermediates before they lead to cancer.
Genomic approaches can provide answers to undiagnosed primary immunodeficiency diseases Nov 15, 2016 A new approach successfully identified disease-causing gene variants in 40 percent of previously undiagnosed patients with primary immunodeficiency diseases.
Researchers develop novel system for cataloging cancer gene variants Nov 15, 2016 A standard way to catalog gene mutations in cancers aims to enhance the use of the information in research and clinical practice.