SingleCellSeqCNV Code
Detection of Copy Number Alterations by Single Cell Sequencing
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Update Feb 2020: Some updates for hg19: * Newer version of HMMcopy 1.28 is now used * 3 more resolutions added * for older scripts, check commit in 2017 Please follow our JoVE protocol paper to run the scripts. by kknouse at mit.edu and jiewu at mit.edu Prerequisites * A unix-like environment with Perl installed. * R with HMMcopy and DNAcopy installed. * SAMTools 0.1.19, BWA 0.6.1, FASTX-Toolkit 0.0.13, Picard 1.94, bowtie 1.0.1 and bedtools 2.17.0. Note: DNAcopy configuration files were generated in the following ways: download mappablility track from ucsc goldenpath: wget http://hgdownload.cse.ucsc.edu/goldenPath/mm9/encodeDCC/wgEncodeMapability/wgEncodeCrgMapabilityAlign40mer.bigWig use bigWigToWig in the kent toolkit to convert it to wiggle: bigWigToWig wgEncodeCrgMapabilityAlign40mer.bigWig wgEncodeCrgMapabilityAlign40mer.wig generate dynamic window: perl GenMapWin.pl wgEncodeCrgMapabilityAlign40mer.wig >500k.dynamic.win.bed and gc profile bedtools getfasta -fi mm9.fa -bed 500k.dynamic.win.bed -fo 500k.dynamic.win.fa perl getGCpercent.pl 500k.dynamic.win.fa >500k.dynamic.win.fa.gc.txt