Open HaniJieunKim opened 3 years ago
Hi, thanks for creating a very useful pacakge!
I'd like to run scone on a scRNA-seq dataset. But I do not have many of the information found in the quality matrix in the tutorial example data (fluidigm).
colnames(qc) [1] "NREADS" [2] "NALIGNED" [3] "RALIGN" [4] "TOTAL_DUP" [5] "PRIMER" [6] "INSERT_SZ" [7] "INSERT_SZ_STD" [8] "COMPLEXITY" [9] "NDUPR" [10] "PCT_RIBOSOMAL_BASES" [11] "PCT_CODING_BASES" [12] "PCT_UTR_BASES" [13] "PCT_INTRONIC_BASES" [14] "PCT_INTERGENIC_BASES" [15] "PCT_MRNA_BASES" [16] "MEDIAN_CV_COVERAGE" [17] "MEDIAN_5PRIME_BIAS" [18] "MEDIAN_3PRIME_BIAS" [19] "MEDIAN_5PRIME_TO_3PRIME_BIAS"
Is there a way to generate this from the scRNA-seq dataset (count data)? I do not have access to the raw pre-aligned data.
Thanks!
Best regards,
Hani
Hi, thanks for creating a very useful pacakge!
I'd like to run scone on a scRNA-seq dataset. But I do not have many of the information found in the quality matrix in the tutorial example data (fluidigm).
Is there a way to generate this from the scRNA-seq dataset (count data)? I do not have access to the raw pre-aligned data.
Thanks!
Best regards,
Hani