Description Usage Arguments Value Examples
Run the mapex algorithm
1 2 3 |
bam_file |
Alignment file for the tumor sample to filter in bam format |
bam_idx |
Index for the alignment in bam_file |
variant_file |
variant call file in maflite, vcf, call_stats, or snp (varscan) format |
variant_file_type |
type of variant call file either maf (default maflite format), vcf (version >= 4.0), call_stats (MuTect1 format), or snp (Varscan2 format) |
blast_out_file |
file name for returned blast hits (default=NULL, do not output scored reads) |
blastn_path |
Path to a local installation of BLASTN |
blast_db_path |
Path to a BLAST database (typically human/mouse reference or human reference) |
blast_threads |
Number to threads to run blast with (default=1) |
min_mapq |
Minimum read mapping quality score (default=1) |
a data frame with four columns; chrom
the chromosome the variant is on,loc
the position of the variant
variant_score
the variant score between 0 and 1, and reason
the variant classification which takes values
mouse
, off_target
, or on_target
.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 | ## Not run:
## file paths and variables
bam <- "/path/to/tumor.bam"
bamidx <- "/path/to/tumor.bai"
variants <- "/path/to/variants.vcf"
blastout <- "/path/to/blastoutput.txt" # Read level blast results, not required
blastpath <- "/path/to/blastn" # if blast is in the users path, just "blastn" here
blastdb <- "/path/to/combined_db"
threads <- 1 # number of threads consumed by blastn
mapq <- 1 # this is the default for minimum mapq score
results <- run_mapex(bam_file=bam,
bam_idx=bamidx,
variant_file=variants,
variant_file_type='vcf',
blast_out_file=blastout,
blastn_path=blastpath,
blast_threads=threads,
min_mapq=mapq)
## End(Not run)
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