Description Usage Arguments Value Author(s) Examples
This function uses a C interface to read the nucleotide counts on each position of a .bam alignment. The counts of both strands are reported separately
and nucleotides below a quality cutoff are masked. It is called by deepSNV
to parse the alignments of the test and control experiments,
respectively.
1 2 |
file |
The name of the .bam file as a string. |
chr |
The chromosome as a string. |
start |
The start position (1-indexed). |
stop |
The end position (1-indexed). |
q |
An optional cutoff for the nucleotide Phred quality. Default q = 25. Nucleotides with Q < q will be masked by 'N'. |
s |
Optional choice of the strand. Defaults to s = 2 (both). |
head.clip |
Should n nucleotides from the head of reads be clipped? Default 0. |
max.depth |
The maximal depth for the pileup command. Default 1,000,000. |
verbose |
Boolean. Set to TRUE if you want to get additional output. |
A named matrix
with rows corresponding to genomic positions and columns for the nucleotide counts (A, T, C, G, -), masked nucleotides (N), (INS)ertions, (DEL)etions, (HEAD)s and (TAIL)s that count how often a read begins and ends at the given position, respectively,
and the sum of alignment (QUAL)ities, which can be indicative of alignment problems.
Counts from matches on the reference strand (s=0) are uppercase, counts on the complement (s=1) are lowercase. The returned matrix has 11 * 2 (strands) = 22 columns and (stop - start + 1) rows.
Moritz Gerstung
1 2 3 4 5 6 | ## Simple example:
counts <- bam2R(file = system.file("extdata", "test.bam", package="deepSNV"), chr="B.FR.83.HXB2_LAI_IIIB_BRU_K034", start = 3120, stop=3140, q = 10)
show(counts)
## Not run: Requires an internet connection, but try yourself.
# bam <- bam2R(file = "http://www.bsse.ethz.ch/cbg/software/deepSNV/data/test.bam", chr="B.FR.83.HXB2_LAI_IIIB_BRU_K034", start = 2074, stop=3585, q=10)
# head(bam)
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