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SolveBio specifications

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Unique identifier OMICS_19323
Name SolveBio
Interface Web user interface
Restrictions to use None
Computer skills Basic
Stability Stable
Registration required Yes
Maintained Yes

SolveBio citations

 (2)
library_books

Exome Pool Seq in neurodevelopmental disorders

2017
Eur J Hum Genet
PMCID: 5865117
PMID: 29158550
DOI: 10.1038/s41431-017-0022-1

[…] washington.edu/) [], REVEL (rare exome variant ensemble learner) (https://sites.google.com/site/revelgenomics/) [], SPIDEX [] (https://www.deepgenomics.com/spidex/) and dbscSNV [] scores (https://www.solvebio.com/data/dbscSNV/) were additionally annotated using SnpSift and the files provided from the respective website. Software and database versions are detailed in Supplementary Table . […]

library_books

Novel exonic mutation inducing aberrant splicing in the IL10RA gene and resulting in infantile onset inflammatory bowel disease: a case report

2016
PMCID: 4730728
PMID: 26822028
DOI: 10.1186/s12876-016-0424-5

[…] lts in the patients affected with familial hemophagocytic lymphohistiocytosis previously [, ].According to the database which predicts splice-altering single nucleotide variants (dbscSNV: https://www.solvebio.com/library/dbscSNV), the IL10RA c.537G > A substitution shows high probability of affecting splicing (the Ada score = 0.99996). This in silico analysis strongly supports our results that the […]


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