Next Generation Sequencing (NGS) Analysis Lab
Genome sequence analysis
Analysis example: Calling SNPs to identify locations where CAPS markers can be designed
Analysis image

Price per sample
Read QC + alignment + SNP calls + CAPS possible SNP calls
2500 + 2500 _cc781905-5cde- 3194-bb3b-136bad5cf58d_ + 3000 _cc781905-5cde-3194-bb3b -136bad5cf58d_ + _cc781905- 5cde-3194-bb3b-136bad5cf58d_1000 = _cc781905-5cde-3194- bb3b-136bad5cf58d_ 9000 Yen
Data you send
・Short read fastq/fasta files
・Reference genome sequence fasta file
Delivery data
・Read quality data (average read length, number of reads, etc.)
・Alignment results (average depth, genome coverage)
・bam file
・List of called SNPs
・List of SNPs that can be converted into CAPS markers
* We can also create files in your desired format and analyze options.
deadline
About 2 weeks after starting QC
Other analysis and reference price list
*Price includes lead QC and alignment. It varies depending on format changes and parsing options.
In addition to the above, we will accept requests for analysis such as long lead analysis as much as possible.