CracTools
CracTools analyzes RNA-Seq and digital gene expression (DGE) datasets to detect transcriptomic features including chimeric transcripts, splice variants, SNPs, and novel transcriptional regions.
Key Features:
- Chimeric Transcript Detection: Identifies chimeric RNA molecules derived from complex transcriptional events.
- Alternative Splicing Identification: Detects splice variants from RNA-Seq datasets to characterize transcript diversity.
- SNP Detection: Performs single nucleotide polymorphism (SNP) calling from transcriptome sequencing data.
- Novel Transcriptional Region Discovery: Integrates RNA-Seq and DGE tag data to identify previously unannotated transcribed regions.
- Genome Annotation Mapping: Maps uniquely aligned tags to the human genome using Ensembl references and categorizes them into protein-coding, antisense, intronic, or intergenic regions.
- Tissue-Specific Transcript Identification: Selects candidate transcripts showing tissue-specific expression patterns.
Scientific Applications:
- Transcriptome Analysis: Supports investigation of transcript structure, alternative splicing, and RNA variation using RNA-Seq and DGE data.
- Gene Regulation Studies: Enables identification of novel transcriptional regions and tissue-specific transcripts.
- Functional Genomics: Facilitates exploration of transcript diversity, genetic variation, and RNA-based regulatory mechanisms.
Methodology:
CracTools maps digital gene expression tags to a reference genome to detect novel transcriptional regions, validates these regions using RNA-Seq reads, and integrates tiling array expression data and species-comparison analyses for transcriptome characterization.
Topics
Details
- Tool Type:
- command-line tool
- Operating Systems:
- Linux
- Programming Languages:
- Perl
- Added:
- 12/18/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Philippe N, Bou Samra E, Boureux A, Mancheron A, Rufflé F, Bai Q, De Vos J, Rivals E, Commes T. Combining DGE and RNA-sequencing data to identify new polyA+ non-coding transcripts in the human genome. Nucleic Acids Research. 2013;42(5):2820-2832. doi:10.1093/nar/gkt1300. PMID:24357408. PMCID:PMC3950697.