Genetic variants interpretation analysis
Budget: €8 – €30 EUR
The job is to filter, analyze and interpret a set of genetic variants
The worker will be provided with a list of genetic variants and will have to filter out the variants that are not real variants (artifacts) or those variants that are not considered relevant or pathogenic. Finally, each variant will be labeled as : LOW-COVERAGE, ARTIFACT, PATHOGENIC or PATHOGENIC (for offspring) or UNCERTAIN.
To do this job the worker needs knowledge of genetics / molecular biology, IGV genetic data viewer and usage of genetic analysis tools and databases such as: Varsome, OMIM, Malacards, HGMD, etc.
For each sample, the worker will have access to:
1) a list of genetic variants (excel file),
2) a VCF file (genetic variants)
3) and BAM file (sequencing data)
Specific instructions for the complete genetic analysis workflow (step by step) will be provided after work acceptance.
The worker will be provided with a list of genetic variants and will have to filter out the variants that are not real variants (artifacts) or those variants that are not considered relevant or pathogenic. Finally, each variant will be labeled as : LOW-COVERAGE, ARTIFACT, PATHOGENIC or PATHOGENIC (for offspring) or UNCERTAIN.
To do this job the worker needs knowledge of genetics / molecular biology, IGV genetic data viewer and usage of genetic analysis tools and databases such as: Varsome, OMIM, Malacards, HGMD, etc.
For each sample, the worker will have access to:
1) a list of genetic variants (excel file),
2) a VCF file (genetic variants)
3) and BAM file (sequencing data)
Specific instructions for the complete genetic analysis workflow (step by step) will be provided after work acceptance.