CRISPR NGS editing check with HISAT2
- Before starting: enable SIMD in your web browser (see Help below).
- This tool is for paired-end fastq files (i.e., xxx_R1_001.fastq.gz and xxx_R2_001.fastq.gz). It uses HISAT2 to find big deletions (treated as introns).
- Please run the three steps below to obtain the indexed BAMs from a list of FASTQ files.
- In the end, you will receive a summary file of indels and all the BAM files to be viewed in IGV.
- No spaces are allowed in input file names.
Junli Zhang 2022-05-01
CRISPR Editing Analysis
- See Help below on your first use
Junli Zhang 2020-11-15
Extract cDNA sequences
- Please paste gene IDs (e.g. TraesCS5A02G391700) or specific cDNA IDs (e.g. TraesCS5A02G391700.2) below.
- Each line is a gene.
Find wheat potential homeologs
- Find potential wheat homeologs (best hit with >90% identity and alignment >60% of the CDS length) and their functions based on Arabidopsis (At) and rice (Os) blast results (top 1 hit).
- Please paste gene IDs (e.g. TraesCS5A02G391700) below. Each line is a gene.
- To start a new job, click the “Clear” button below and resubmit (faster than refreshing the page).
Junli Zhang 2024-07-23
Kronos-Chinese Spring Gene ID conversion
- Match the genes in CS RefSeq v1.1 annotation HC with Kronos v1.0 annotation (best hit with >97% identity and alignment length > 100 bp).
- Some genes may have multiple hits or not on the same chromosome. Select with your own eyes based on chromosome matches and %identity.
- Please paste gene IDs (e.g., TraesCS5A02G391700) or transcript IDs (e.g., TraesCS5A02G391700.1; the tool will convert them to gene IDs). Each line is a gene.
- The output will be the best-matching transcript IDs.
Junli Zhang 2024-07-26