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Publication Details

Results for Yin2020:

Summary
Title Next Generation Sequencing of 134 Children with Autism Spectrum Disorder and Regression
AuthorsYin, J., Chun, C.-A., Zavadenko, N.N., Pechatnikova, N.L., Naumova, O.Y., Doddapaneni, H.V., Hu, J., Muzny, D.M., Schaaf, C.P., Grigorenko, E.L.
TechnologyTargeted sequencing
Variant sourceTable 2
Cohortscohort from a specialized central medical center in Moscow, Russia
Designsimplex
URLhttps://dx.doi.org/https://www.mdpi.com/2073-4425/11/8/853
Pubmed32722525
Subject count15
The number of subjects for this study could not be determined directly from the variant data; the value given is that reported by the authors in the publication.
Variant event count18
Curation notesView
Breakdown by exonic function
FunctionVariant Count
nonsynonymous SNV17
splicing1

What am I looking at?

Summary: Information from the literature piece (e.g. Author, Publisher, DOI) and the study experimental design (e.g. sample size, source of probands, sequencing technology.) For a full list of sources of variants, be sure to check out the publications page. Documentation and description of our work can be found on the help page.

Breakdown by exonic function: We annotated the variants with an effect prediction using ANNOVAR. The functions are categories of variants, such as frameshift variants (i.e. frameshift_elongation (SO:0001909)), loss/gain of stop codon, SNVs and non-frameshift variants. See the full list of possible annotations for exonic variants in the documentation.