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_____________________________________________________________________Sampling time after treatment

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  • RNA-seq analysis
  • DNA-seq analysis
  • Genetic variation
  • ChiP-seq analysis
  • ATAC-seq analysis
  • Single cell Analysis
    • Single cell GEX
    • Single cell ATAC-Seq
    • Single cell
    RNA
    • GEX + Hashing
    • CITE-Seq
    • Multiome (GEX + ATAC-Seq)
    • Single cell GEX + BCR/TCR
    • Other -__________
  • Small-RNA analysis
  • Functional/pathway analysis
  • Methylation analysis
  • Proteomics
  • Integration
  • Other: (comments) -__________



Sample FeaturesEstimating replicates needed

Sample

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Cells/tissue description (gender, type of cells, genetic manipulation, FAX, treatment..) 

Species ___________________________________________________________________

Gender____________________________________________________________________

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Tissue description____________________________________________________________

_____________________________________________________________________________

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Cell types____________________________________________________________________

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Genetic Manipulation____________________________________________________________

_____________________________________________________________________________

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Lab manipulation (FACS, nuclei)_____________________________________________________

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Other information_______________________________________________________________


Estimating replicates needed

  • Sample Purity (% of cells which are of interest, reproducibility of this percentage)

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  • Genetic purity  cell line (at least 3 replicates)
     whole organism inbreed (at least  3 replicates)  other (even 10 replicates)

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  • Pooling – avoid if possible. At least 5 samples. Need to have 3 replicates.

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  • If there is small variance between treatments more replicates needed  yes  no

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If not – perform each replicate of the experiment at the same time.

 

For single cell analysis estimation of abundancy of cell population of interest (in percent)

______________________________________________________________________________

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Summary:

Platform name:                ILLUMINA     PACBIO    NANOPORE     MS

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                                          Length of the read _________                 

Number of reads reads_________________________________________________________________

Protocol type ___________________________________________________________________                                                                              


Duration for first analysis:

Evaluation of project size for bioinformatics analysis: Low/Medium/LargeDuration (Relative to data received date):

Duration  for initial analysis :_____________________________________________

Expected date when the sequences will be ready :______________________________________