AnNCR-SNP integrates data from various sources, allowing the user to investigate the potential effects of variants in non-coding regions of the human genome. AnNCR-SNP consists of a database containing data on all non-coding elements and two main programs: manager and finder. The manager program is responsible for creating the local data-base, and the finder program receives the user queries in order to search in the local database and retrieve information. The user can find information about various regu-latory elements, such as TFBs, open chromatin, histone modification and methyla-tion sites, information about SNPs from dbSNP and gene information from RefSeq.

Required Ruby Version

>= 0

Authors

Elena Rojano, Pedro Seoane

Versions

  1. 0.1.7

    1. source

      1. 0.1.7 source September 28, 2016 (27 KB)
  2. 0.1.6

    1. source

      1. 0.1.6 source July 25, 2016 (20 KB)
  3. 0.1.5

    1. source

      1. 0.1.5 source July 22, 2016 (20 KB)
  4. 0.1.4

    1. source

      1. 0.1.4 source July 20, 2016 (20 KB)
  5. 0.1.3

    1. source

      1. 0.1.3 source July 20, 2016 (19 KB)
Show all versions (8 total)

SHA 256 checksum

← Previous version