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FDNA and Genome Medical Improve Access to Critical Diagnostic Services for Children in Medically...
WKBN 27 Youngstown· 16 hours ago...interventions for children with developmental conditions SOUTH SAN FRANCISCO, Calif. and ATLANTA, May 20, 2024 /PRNewswire/ -- FDNA Inc, the leader in the early detection of rare genetic diseases, and Genome Medical, the nation's leading telehealth provider of genetic services, have partnered to...
Revolutionary Genetics Research Shows RNA May Rule Our Genome - Slashdot
Slashdot· 6 days agoIn 2012 the geneticist, now at Cold Spring Harbor Laboratory in New York State, was one of a few hundred colleagues who were simply trying to put together a compendium of human DNA functions ...
Optical genome mapping unveils hidden structural variants in neurodevelopmental disorders -...
Nature· 5 days agoWhile short-read sequencing currently dominates genetic research and diagnostics, it frequently falls short of capturing certain structural variants (SVs), which are often implicated in the ...
A genome-wide association study identifies a locus associated with knee extension strength in older...
Nature· 23 hours agoA genome-wide association study on knee extension strength in 3452 persons of Japanese ancestry 60 years old and above identifies a significant association at a single locus ...
Ambry Genetics, Pacific Biosciences to Sequence up to 7K Human Genomes for Rare Disease Study
GenomeWeb News· 5 days agoAmbry Genetics and Pacific Biosciences said Wednesday that they will sequence up to 7,0000 human whole genomes over three years using long-read technology ...
Ambry Genetics and PacBio Announce Collaboration to Sequence Up to 7,000 Human Genomes Aimed at...
Morningstar· 6 days agoALISO VIEJO, Calif. and MENLO PARK, Calif., May 15, 2024 /PRNewswire/ --Ambry Genetics, a prominent leader in clinical genomic testing and a subsidiary of REALM IDx, Inc., ...
Nature Vs Nurture In Beethoven’s Genome
Hackaday· 4 days agoWhen it comes to famous musicians, Beethoven is likely to hit most top ten charts. Researchers recently peered into his genome to see if they could...
The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of...
Nature· 4 days agoEach family presented to a different clinical centre, and following diagnostic exome or genome sequencing, was found to harbour two variants in MEGF8 consistent with a causal ...
Chromatin modifications integrate cis genomic context to instruct transcriptional outputs - Nature ...
Nature· 23 hours agoBy developing a modular system for precision epigenome editing, we were able to delineate the causal and quantitative role of chromatin modifications in transcription regulation. The precise ...
Sweet trade-offs: Unraveling the genetic puzzle of strawberry flavor and yield
Phys.org· 12 hours agoUnderstanding the genetic basis of sugar accumulation is crucial for breeding programs aiming to meet the increasing demand for strawberries with superior taste and quality. Based on these challenges ...