Releases: tjiangHIT/cuteSV
Releases · tjiangHIT/cuteSV
Version update
- fix bugs in resolving reference genomes
- modify several dependencies and remove some useless dependencies
- update several evaluation scripts
Version update
- Speed up both SV discovery calling and force calling comprehensively.
- Upgrade the force-calling module.
- Update several functions and regulations.
Version update
- Fix the error of missing min_size parameter.
- Fix the missing signatures in duplication clustering.
Version update
- Fix several errors in signature extraction.
- Filter low quality reads in the statistics of reference reads.
- Modify the rule of merging signatures on the same read.
- Modify the cluster rule of insertions and deletions in force calling.
Version update
- Fix an error in handling strand in force calling.
- Speed up the genotype module of discovery calling. The comparison results on various datasets are as follows.
cuteSV (previous) | cuteSV2 (latest) | |
---|---|---|
CCS | 900.37s | 261.77s |
CLR | 3620.00s | 2644.94s |
ONT | 2893.08s | 1264.26s |
Version upgrade
cuteSV (v2.0.0):
- Upgrade the force-calling module.
- Add --remain_reads_ratio parameter in order to generate a highly accurate record by discarding a few signatures.
- Fix several bugs in inversion and translocation calling.
- Remove the redundant operations in the signature extraction and accelerate the whole analysis.
- Streamline the translocation output when performing force-calling.
- Modify the signature matching rule.
- Modify the sequence of the inserted allele.
v1.0.13
- Modify the breakpoints of alternative allele and reference allele.
- Fix an initialization error that will reproduce wrong diploid-assembly-based SV call.
v1.0.12
cuteSV (v1.0.12):
- Add Allele frequency (AF) info in the outputs.
- Fix an index error when force calling BND variants.
- Modify the parameter of --max_size and enable to report full length of SVs.
cuteSV-v1.0.11
cutesv (v1.0.11):
- Add a script for post-processing typically cuteSV callsets from assembly-based alignments to generate the diploid-assembly-based SV calls.
- Give a wiki page for helping uses to achieve assembly-based SV calling.
- Improve acquirement of inserted sequence in a read whose primary alignment contains hardclips.
- Improve the performance of force calling.
- Enable cuteSV to output allele sequences when performing force calling with the VCF generated from other callers.
- Fix bugs to avoid the error raised by abnormal SV type.
- Update the sort commands used in cuteSV.
- Update the parameter of --max_split_parts.
cuteSV-v1.0.10
cutesv (v1.0.10):
- Fix a bug leading to calculate wrong TRA positions.
- Add a file format conversion script that enable to transfer the vcf file to bedpe file.
- Involve several clustering-and-refinement strategies in force calling function.
- Assessed the performance of force calling with Giab HG002 sample datasets (including CLR, CCS, and ONT platforms).