This data describes the screening results of 400 Brazilian blood donors, using two differents platforms:OpenArray and Real Time PCR FRET, for detection of 7 SNPS (four related to thrombophilia and 3 r
Whole-exome sequencing (WES) can identify causative mutations in hereditary diseases. However, WES data might have a large candidate variant list, including false positives. Moreover, in families, it
