Unlock your biological data


Allele-specific binding software tools | ChIP sequencing data analysis

Detection of allelic imbalances in ChIP-Seq reads is a powerful approach to identify functional non-coding single nucleotide variants (SNVs), either polymorphisms or mutations, which modulate the affinity of transcription factors for chromatin.

Source text:
(Bailey et al., 2015) ABC: a tool to identify SNVs causing allele-specific transcription factor binding from ChIP-Seq experiments. Bioinformatics.

1 - 6 of 6 results
filter_list Filters
settings_input_component Operating System
tv Interface
computer Computer Skill
copyright License
1 - 6 of 6 results
0 - 0 of 0 results
1 - 4 of 4 results
filter_list Filters
computer Job seeker
Disable 1
person Position
thumb_up Fields of Interest
public Country
language Programming Language
1 - 4 of 4 results