GTB – an online genome tolerance browser

Background Accurate methods capable of predicting the impact of single nucleotide variants (SNVs) are assuming ever increasing importance. There exists a plethora of in silico algorithms designed to help identify and prioritize SNVs across the human genome for further investigation. However, no tool...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:BMC bioinformatics Ročník 18; číslo 1; s. 20
Hlavní autoři: Shihab, Hashem A., Rogers, Mark F., Ferlaino, Michael, Campbell, Colin, Gaunt, Tom R.
Médium: Journal Article
Jazyk:angličtina
Vydáno: London BioMed Central 06.01.2017
BioMed Central Ltd
Springer Nature B.V
Témata:
ISSN:1471-2105, 1471-2105
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Popis
Shrnutí:Background Accurate methods capable of predicting the impact of single nucleotide variants (SNVs) are assuming ever increasing importance. There exists a plethora of in silico algorithms designed to help identify and prioritize SNVs across the human genome for further investigation. However, no tool exists to visualize the predicted tolerance of the genome to mutation, or the similarities between these methods. Results We present the Genome Tolerance Browser (GTB, http://gtb.biocompute.org.uk ): an online genome browser for visualizing the predicted tolerance of the genome to mutation. The server summarizes several in silico prediction algorithms and conservation scores: including 13 genome-wide prediction algorithms and conservation scores, 12 non-synonymous prediction algorithms and four cancer-specific algorithms. Conclusion The GTB enables users to visualize the similarities and differences between several prediction algorithms and to upload their own data as additional tracks; thereby facilitating the rapid identification of potential regions of interest.
Bibliografie:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ISSN:1471-2105
1471-2105
DOI:10.1186/s12859-016-1436-4