SWIFT-seq report

Read processing:

Total reads:107,839,114
Number of reads post-trimming:105,521,554
Reads with 0 barcodes (%):1.27%
Reads with 1 barcodes (%):2.87%
Reads with 2 barcodes (%):5.29%
Reads with 3 barcodes (%):90.57%
Reads with all 3 barcodes:93,882,175
Reads excluded*:68.09% (63,925,527 out of 93,882,175 reads)
Final number of reads:29,956,648

(Note: An additional 1,868,348 reads were filtered out during barcode identification)

*Reads mapped to an exclusion index (e.g. if mapping to an exclusion index containing ribosomal RNA, this percentage is ribosomal RNA content).

Alignment results (STARsolo):

Number of input reads 29,956,648
Uniquely mapped 66.94%
Uniquely mapped within genes (including introns) 59.06%
Uniquely mapped within genes (excluding introns) 29.64%
Sequencing saturation (1 - Numi / Nreads) 2.78%
Unmapped/Multimapped reads
  • Multimapped (multiple loci): 4.49%
  • Multimapped (too many loci): 0.29%
  • Unmapped (too many mismatches): 0.00% (0 reads)
  • Unmapped (too short): 28.24%
  • Unmapped (other): 0.05% (13,963 reads)
  • Chimeric reads: 0.00% (0 reads)

Kallisto pseudoalignment:

Number of input reads 29,956,648
Percent pseudoaligned 75.4%
Percent pseudoaligned to unique transcripts 35.3%

Analysis

Per-sample summary

SampleTotal readsUniquely mapped (%) – STARsoloPseudoalignment (%) – kallisto
humanmouse12pt5KA14,924,00869.97%76.6%
humanmouse25K15,032,64063.93%74.1%

Barcode representation