Biotexcel
@Biotexcel
Genomics, Biomarkers and Diagnostics from Patient Perspectives - Knowledge Dissemination and Research Advocacy
قد يعجبك
Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level - ow.ly/i1zE30ruUYg
The role of gene to gene interaction in the breast’s genomic signature of pregnancy - ow.ly/Yv0G30ruUYf
Chimeric synthetic reference standards enable cross-validation of positive and negative controls in SARS-CoV-2 molecular tests - ow.ly/7xxL30ruUYe
Long-read whole-genome sequencing identified a partial MBD5 deletion in an exome-negative patient with neurodevelopmental disorder - ow.ly/uoqA30ruUYd
Detection of genetic variation and base modifications at base-pair resolution on both DNA and RNA - ow.ly/zf8N30ruUYc
Single cell sequencing reveals endothelial plasticity with transient mesenchymal activation after myocardial infarction - ow.ly/6DBA30ruUYb
CDK19-related disorder results from both loss-of-function and gain-of-function de novo missense variants - ow.ly/p8fi30ruacj
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder - ow.ly/prbW30ruaci
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity - ow.ly/127430ruach
Mutation load at a mimicry supergene sheds new light on the evolution of inversion polymorphisms - ow.ly/wV8Z30ruacg
Opposing immune and genetic mechanisms shape oncogenic programs in synovial sarcoma - ow.ly/GsIk30ruacf
Participant mothers’ attitudes toward genetic analysis in a birth cohort study - ow.ly/43wL30ruace
nature.com
Participant mothers’ attitudes toward genetic analysis in a birth cohort study
Journal of Human Genetics - Participant mothers’ attitudes toward genetic analysis in a birth cohort study
Liquid biopsy enters the clinic — implementation issues and future challenges - ow.ly/ciBw30rtyN0
Repeat DNA-PAINT suppresses background and non-specific signals in optical nanoscopy - ow.ly/r9hj30rtyMY
Whole genomic sequencing based genotyping reveals a specific X3 sublineage restricted to Mexico and related with multidrug resistance - ow.ly/R6pR30rtyMX
Estimation of the carrier frequencies and proportions of potential patients by detecting causative gene variants associated with autosomal recessive bone dysplasia using a whole-genome reference panel of Japanese individuals - ow.ly/DVls30rt3zz
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قد يعجبك
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Genome Medicine
@GenomeMedicine -
Front Line Genomics
@FLGenomics -
Integrated DNA Technologies
@idtdna -
McDonnell Genome Institute, WashU Medicine
@GenomeInstitute -
UC Santa Cruz Genomics Institute
@ucscgenomics -
Strand Life Sciences
@StrandLife -
Manuel Corpas
@manuelcorpas -
Fios Genomics
@fiosgenomics -
Personalis, Inc.
@PersonalisInc -
Fabric Genomics
@FabricGenomics -
Dale Yuzuki
@DaleYuzuki
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