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SolveBio specifications


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


Exome Pool Seq in neurodevelopmental disorders

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

[…] [], REVEL (rare exome variant ensemble learner) ( [], SPIDEX [] ( and dbscSNV [] scores ( were additionally annotated using SnpSift and the files provided from the respective website. Software and database versions are detailed in Supplementary Table . […]


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

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:, 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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