Alignment / TopHat2 for single end reads and own genome

Description

This tool aligns Illumina single end RNA-seq reads to a genome provided as a FASTA file. You need to supply the reads in one or more FASTQ files.

Supplying a GTF file containing known gene and exon locations is recommended, because it improves the alignment process.

Parameters

Library type (fr-unstranded, fr-firststrand, fr-secondstrand) [fr-unstranded]
When GTF file is used, ignore novel junctions (yes, no) [yes]
Base quality encoding used (phred+33, phred+64) [phred+33]
How many hits is a read allowed to have (1-1000000) [20]
Number of mismatches allowed in final alignment [2]
Minimum anchor length (3-1000) [8]
Maximum number of mismatches allowed in the anchor (0, 1, 2) [0]
Minimum intron length [70]
Maximum intron length [500,000]

Details

TopHat2 maps Illumina RNA-Seq reads to a genome in order to identify exon-exon splice junctions. The alignment process consists of several steps. If annotation is available as a GTF file, TopHat will extract the transcript sequences and use Bowtie2 to align reads to this virtual transcriptome first. Only the reads that do not fully map to the transcriptome will then be mapped on the genome. The reads that still remain unmapped are split into shorter segments, which are then aligned to the genome. Segment mappings are used to find potential splice sites. Sequences flanking a splice site are concatenated, and unmapped segments are mapped to them. Segment alignments are then stitched together to form whole read alignments.

The "anchor length" means that TopHat2 will report junctions spanned by reads with at least this many bases on each side of the junction. Note that individual spliced alignments may span a junction with fewer than this many bases on one side. However, every junction involved in spliced alignments is supported by at least one read with this many bases on each side. By default no mismatches are allowed in the anchor, but you can change this.

TopHat2 will ignore donor-acceptor pairs which are closer than the minimum intron length or further than the maximum intron length apart.

After running TopHat2, Chipster indexes the BAM file using the SAMtools package. This way the results are ready to be visualized in the genome browser.

If your RNA-seq data was produced with a stranded/directional protocol, it is important that you select the correct strandedness option in the parameter "Library type":

fr-unstranded (Standard Illumina).
fr-firststrand (dUTP, NSR, NNSR): The right-most end of the fragment (in transcript coordinates) is sequenced. Equivalently, it is assumed that only the strand generated during first strand synthesis is sequenced. For example Illumina TruSeq Stranded Total RNA Sample Prep Kit is a dUTP method.
fr-secondstrand (Ligation, Standard SOLiD): The left-most end of the fragment (in transcript coordinates) is sequenced. Equivalently, it is assumed that only the strand generated during second strand synthesis is sequenced.

You can read more about stranded data here.

Output

This tool returns the following files:

tophat.bam: BAM file containingthe alignments.
tophat.bam.bai: Index file for the BAM file.
tophat-summary.txt: Summary of the alignment results.
junctions.bed: Each junction consists of two connected BED blocks, where each block is as long as the maximal overhang of any read spanning the junction. The score is the number of alignments spanning the junction.

In cases where Tophat2 for some reason fails, file tophat2.log is returned instead.

Reference

This tool is based on the TopHat package. Please cite the following article:

Kim D, Petrtea G, Trapnell C, et al. TopHat2: accurate alignments of transcriptomes in the presence of insertions, deletions and gene fusions. Genome Biology (2013) 14: R36.