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UnknownGene content, phage cycle regulation model and prophage inactivation disclosed by prophage genomics in the <i>Helicobacter pylori</i> Genome Project.
Not available
S-EPMC11321410 | biostudies-literature
GenomicsGenome Wide Association for Asthma and Lung Function

The SNP Typing for Association with Multiple Phenotypes from Existing Epidemiologic (STAMPEED) asthma project includes subjects with asthma and controls from the Chicago Asthma Genetics Study (CAG), NHLBI multicenter Severe Asthma Research Program (SARP) and NHLBI Collaborative Studies ...

phs000355.v1.p1 | EGA
UnknownDeepISLES: a clinically validated ischemic stroke segmentation model from the ISLES'22 challenge
Not available
S-EPMC12335569 | biostudies-literature
UnknownEpidemiology of anal human papillomavirus infection and high-grade squamous intraepithelial lesions in 29 900 men according to HIV status, sexuality, and age: a collaborative pooled analysis of 64 studies.
Not available
S-EPMC8408042 | biostudies-literature
UnknownBi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.
Not available
S-EPMC6507039 | biostudies-literature
UnknownNewborn screening for severe combined immunodeficiency in 11 screening programs in the United States.
Not available
S-EPMC4492158 | biostudies-literature
UnknownLate Window Imaging Selection for Endovascular Therapy of Large Vessel Occlusion Stroke: An International Survey.
Not available
S-EPMC12778602 | biostudies-literature
UnknownWhole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children With Asthma.
Not available
S-EPMC6904857 | biostudies-literature
UnknownHuman subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex.
Not available
S-EPMC5540813 | biostudies-literature
Genomicsena-DATASET-GoT2D/T2D-GENES-09-07-2016-02:03:47:226-1135 - samples
The GoT2D study includes ~2800 samples, half T2D cases and half T2D controls, of Northern European ancestry sequenced over 3 three technologies: deep whole exome sequencing, low-pass (4x) whole genome sequencing, and OMNI 2.5M genotyping. Samples were ascertained to be phenotypically "extreme" (e.g....
EGAD00001002247 | EGA
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