Blue:RNA-Seq Experiments:11072016: Difference between revisions
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#1x Lysis + 0.1% Triton X-100 | #1x Lysis + 0.1% Triton X-100 | ||
#1x Lysis + 0.2% Triton X-100 | #1x Lysis + 0.2% Triton X-100 | ||
#1x Lysis + 0.1% Triton X-100 + PolydidC | #1x Lysis + 0.1% Triton X-100 + PolydidC | ||
#1x Lysis + vortex 30s | #1x Lysis + vortex 30s | ||
#NTC | #NTC | ||
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#1% Triton X-100: | #1% Triton X-100: | ||
## | ##2ul 10% + 18ul dH2O | ||
#0.5% Triton X-100 + PolydIdC: | #0.5% Triton X-100 + PolydIdC: | ||
##1ul 10% + 13.9ul PolydIdC + 5.1ul dH2O | ##1ul 10% + 13.9ul PolydIdC + 5.1ul dH2O | ||
Revision as of 20:29, 7 November 2016
Overview
- Test Smarter v4 chemistry lysis conditions for nuclei
- Initial C1 runs on v4 chemistry showed lower genome mapping rates, therefore it is possible that the new lysis conditions (i.e. 1x lysis buffer) are not optimal for nuclei
- The HT C1 chips run v3 chemistry and have the same lysis conditions, therefore we want to determine whether we can optimize lysis for nuclei
- Test whether polydIdC has any beneficial effect on the new V4 chemistry
Experiment
- Tube control (100 nuclei) test conditions:
- 1x Lysis
- 1x Lysis + 0.1% Triton X-100
- 1x Lysis + 0.2% Triton X-100
- 1x Lysis + 0.1% Triton X-100 + PolydidC
- 1x Lysis + vortex 30s
- NTC
- note: to mimic C1 conditions, lysis buffer will be added without mixing to cells unless stated
- Procedure (as per tube control protocol for V4):
- Modifications to Lysis Buffer (no PolydIdC):
- C1 loading reagent + ERCC | 0.5ul
- 3' Smart-seq CDS primer IIA | 1.2ul
- 10x Reaction buffer | 1.3ul
- Nuclease Free Water | 5ul
- Combine:
- Lysis Mix | 2ul
- Triton X-100 +/- PolydIdC | 0.5ul
- TritonX100 PolydIdC mixes:
- 0.5% Triton X-100:
- 1ul 10% + 19ul dH2O
- 1% Triton X-100:
- 2ul 10% + 18ul dH2O
- 0.5% Triton X-100 + PolydIdC:
- 1ul 10% + 13.9ul PolydIdC + 5.1ul dH2O