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Compatibility with 10X CNV output #22

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kieranrcampbell opened this issue Aug 8, 2018 · 5 comments
Open

Compatibility with 10X CNV output #22

kieranrcampbell opened this issue Aug 8, 2018 · 5 comments
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enhancement New feature or request

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@kieranrcampbell
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When uptake of the 10X single-cell CNV system becomes widespread we should ideally support whatever they output to make it as easy as possible for users. We will also need some sort of heuristic alignment of breakpoints if 10X software doesn't produce this.

Andrew McPherson has a joint HMM that segments all the cells simultaneously that seemed to partially solve the alignment issue.

@kieranrcampbell kieranrcampbell added the enhancement New feature or request label Aug 8, 2018
@alexandrebouchard
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Hey Kieran, if you send me data you found during the meeting today I can have a look at adding an option for their data formats.

@kieranrcampbell
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kieranrcampbell commented Aug 19, 2018 via email

@alexandrebouchard
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As Kieran mentioned today, 10X has bins that are 4x coarser. Likely to have more events merged together.

@kieranrcampbell
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Reference for this

For an approximately diploid human sample we recommend a sequencing depth of 750,000 read-pairs per cell. At this depth, the metric median effective reads per 1Mbp is between 350-400, and we expect to be able to detect single cell copy number events in the size range 1-2 megabases (and upwards) with high sensitivity and positive predictive value. In groups of 10 or more cells we expect to be able to detect copy number events in the 100-200 kilobase (and upwards) with high sensitivity and positive predictive value.

@alexandrebouchard
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Thanks!

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