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[ 源代码: mosdepth  ]

软件包:mosdepth(0.3.6+ds-1 以及其他的)

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BAM/CRAM depth calculation biological sequencing

Many small reads are produced by high-throughput "next generation" sequencing technologies. The final sequence is derived from how these reads are overlapping towards a consensus. The more reads are covering/confirming parts of a nucleotide seq, the higher the confidence is. Too many reads would be indicative of e.g. repeats in the genome.

mosdepth can output:

 *  per-base depth about 2x as fast samtools depth--about 25 minutes
    of CPU time for a 30X genome.
 *  mean per-window depth given a window size--as would be used for
    CNV calling.
 *  the mean per-region given a BED file of regions.
 *  a distribution of proportion of bases covered at or above a given
    threshold for each chromosome and genome-wide.
 *  quantized output that merges adjacent bases as long as they fall
    in the same coverage bins e.g. (10-20)
 *  threshold output to indicate how many bases in each region are
    covered at the given thresholds.
when appropriate, the output files are bgzipped and indexed for ease of use.

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下载 mosdepth

下载可用于所有硬件架构的
硬件架构 版本 软件包大小 安装后大小 文件
amd64 0.3.6+ds-1 166.4 kB585.0 kB [文件列表]
arm64 0.3.6+ds-1 160.2 kB597.0 kB [文件列表]
armel 0.3.6+ds-1 149.7 kB537.0 kB [文件列表]
armhf 0.3.6+ds-1 152.9 kB417.0 kB [文件列表]
i386 0.3.6+ds-1 180.4 kB624.0 kB [文件列表]
mips64el 0.3.6+ds-1 153.4 kB652.0 kB [文件列表]
ppc64 (非官方移植版) 0.3.6+ds-1 174.4 kB726.0 kB [文件列表]
ppc64el 0.3.6+ds-1 176.5 kB725.0 kB [文件列表]
riscv64 0.3.6+ds-1 167.7 kB497.0 kB [文件列表]
sparc64 (非官方移植版) 0.3.3+ds-1 134.0 kB543.0 kB [文件列表]