Releases: haowenz/chromap
Chromap v0.3.2
Chromap v0.3.1
v0.3.0 (r509)
Output peak-based QC metrics, such as estimated fraction of reads in peaks (FRiP) values, without peak callings for single-cell data (e.g. scATAC-seq) in the summary file (--summary option)
v0.2.7 (r494)
v0.2.6 (r486)
- Support wildcard in file names. #58
- Fix the TLEN overflow issue for SAM output on Hi-C data. #139
- Remove the internal sort for --read-format option. #136
- Fix a bug in the summary file for SAM format output, where duplicate, unmapped, lowmapq read pairs are counted twice. #143
- Add the duplicate count in the bulk data BED output. #145
v0.2.5 (r473)
- Add the option "--summary" to output the mapping statistics (e.g. total reads, duplicated read, unmapped reads and low-mapq reads) summarized at the bulk or single-cell level (#107).
v0.2.4 (r467)
v0.2.3 (r407)
This release provides a new feature that allows users to further customize the barcodes based on the original barcode input file (#42). Now multiple ranges for each sequence in the input sequence file can be given in `--read-format' option. For each sequence, Chromap will extract the specified subsequences in the ranges and combine those subsequences as a barcode.
Note that this release does not change mapping results for any input but only provides this new feature.
v0.2.2 (r388)
This release fixed the following bugs.
- When using
--read-format, the quality scores are wrongly complemented, which is fixed now. - The segfault caused by adapter trimming in #46 is fixed.
This release also improved barcode processing.
- Barcode with Ns are now not used for estimating barcode frequency.
- When correcting the barcode, its Ns are corrected first.
This release improve adapter trimming. It can now properly handle the case when one end of the read pair is a subsequence of the other in #88.
The results on mapping paired-end scATAC-seq reads would change slightly. If you previously used Chromap to process your paired-end scATAC-seq data, you may want to rerun it.
