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Rare frequency functional variants in these healthy individuals will be studied with respect to the genetic health of the participants and loss-of-function analysis of human genes. This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/" --sample-alias=sc_autozygELGH7221860,sc_autozygELGH7221868,sc_autozygELGH7221876,sc_autozygELGH7221885,sc_autozygELGH7221893,sc_autozygELGH7221901,sc_autozygELGH7221910,sc_autozygELGH7221919,sc_autozygELGH7221928,sc_autozygELGH7221939,sc_autozygELGH7221950,sc_autozygELGH7221852,sc_autozygELGH7221861,sc_autozygELGH7221869,sc_autozygELGH7221877,sc_autozygELGH7221886,sc_autozygELGH7221894,sc_autozygELGH7221902,sc_autozygELGH7221911,sc_autozygELGH7221920,sc_autozygELGH7221929,sc_autozygELGH7221941,sc_autozygELGH7221954,sc_autozygELGH7221853 --threads=8 --output-file=- --compression-level=0 PN:bambi DS:Convert Illumina BCL to BAM or SAM file @PG ID:bamadapterfind PN:bamadapterfind CL:/software/sciops/pkg/biobambam2/2.0.79/bin/bamadapterfind level=0 PP:bambi VN:2.0.79 @PG ID:bambi.1 PN:bambi 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