Man pages for BartBroeckx/Mendelian
Variant Analysis for Mendelian Disorders
| annot | Annotate variant data frame. |
| CLCfile | Prepare CLC output for filtering |
| CLCfile1 | CLCfile1 documentation A dataset containing 8 variants... |
| CLCfile2 | CLCfile2 documentation A dataset containing 9 variants... |
| commonvar | Combining the output of several filters. |
| gDom | Variant filtering with dominant inheritance considering... |
| genBED | genBED documentation A bed file containing genes used to... |
| gRec | Variant filtering with recessive inheritance considering... |
| nDom | Variant filtering with dominant inheritance |
| nRec | Variant filtering with recessive inheritance |
| prepvar | Preparing variant database. |
| prepvarpar | Preparing variant database (parallel). |
| SNP | SNP documentation A dataset containing 472 variants from the... |
| test | test documentation An example of a VCF file. |
| varfilter | Filtering variants from a database. |
| VCFfile | Prepare VCF file for filtering. |
