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Thread | Thread Starter | Forum | Replies | Last Post |
Bias and quality using Ion Torrent Proton for RNA-seq | tlorin | General | 0 | 10-07-2014 02:16 AM |
Look for somatic mutation from Ion Proton Exome Sequencing | lethalfang | Bioinformatics | 2 | 09-11-2014 02:42 AM |
Ion Proton and fungal ITS amplicon sequencing. | akinadetutu | Ion Torrent | 2 | 04-12-2014 12:57 AM |
Sequencing Ion PGM libraries using Ion Proton | MissDNA | Ion Torrent | 2 | 03-03-2014 12:07 PM |
hybridization failure- Target exome sequencing Ion proton | vandy | Ion Torrent | 2 | 07-30-2013 03:12 AM |
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#1 |
Junior Member
Location: Russia Join Date: Mar 2015
Posts: 3
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Hi
I have NGS exome sequencing results (fastq file) and I generated FASTQC report for it, and AFAICS the result looks like sequencing data is suboptimal. I am alien to the field, and would like to get community's opinion on how good/bad/typical the data actually is. The lab told they used Ion Proton and followed ACMG standards - no more details, don't know chemistry kit. The report below, and thanks in advance. FASTQC version 0.11.2 File type: Conventional base calls Encoding: Sanger / Illumina 1.9 Total Sequences: 33803990 Sequences flagged as poor quality: 0 Sequence length: 8-376 %GC: 48 Per base sequence quality, Error icon ![]() Per sequence quality scores, Warning icon ![]() Per base sequence content, Error icon ![]() Per sequence GC content, Warning icon ![]() Per base N content, OK icon ![]() Sequence Length Distribution, Warning icon ![]() Sequence Duplication Levels, OK icon ![]() Overrepresented sequences, OK icon No overrepresented sequences Adapter Content, OK icon ![]() Kmer Content, Error icon ![]() ![]() |
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#2 |
Senior Member
Location: East Coast USA Join Date: Feb 2008
Posts: 7,080
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See this thread for additional information about Q-scores on Ion platform: http://seqanswers.com/forums/showthread.php?t=33555
Your data may be of good quality based on the discussion in thread above. |
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