Variant callers for single cell WGS
Which variant callers can be used for the detection of indels, SNPs, and CNVs in single-cell whole genome sequencing, where the sequencing was done using Illumina NovaX ?
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Of course you can run a cell ranger generated bam through a variant calling program or pipeline, but single cell sequencing is so spotty, and often biased to one end or the other of the transcript, you are going to miss a lot.
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We use the MDA method to amplify the DNA. Library prep : DNA fragmentation - Repair - adaptor Ligation - size selection- pcr (optional) - purification
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