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

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

Comment