Version changelog 4.2.0 SMRT Link v25.1 release Update PM
to show platform name Update RGID
to match molecule
read name for groupdedup
/ dedup
4.1.0 Update minimap2 to version 2.26 SMRT Link v13.0 release 4.0.0 Rename isoseq3
to isoseq
Add new tool isoseq cluster2
Update --max-5p-diff
default value for isoseq collapse
Add X
design option to isoseq tag
to remove TSO sequences 3.8.2 Update groupdedup
to output consistent molecular IDs across runs Bug fix updating rc
and gp
tags to passing for subset of correct
reads 3.8.1 Real-cell --method
and --percentile
options added to correct
3.8.0 collapse
allows isoforms with 5p degradation to collapse by default --do-not-collapse-extra-5exons
added to collapse
collapse
max 5p and 3p distances can be set in CLI using --max-5p-diff
and --max-3p-diff
Real-cell annotation in correct
using rc
tag Real-cell filtering in groupdedup
, dedup
, and collapse
3.7.0 Adding bcstats
, correct
, and groupdedup
to CLI bcstats
emits frequency statistics for 10x barcodes correct
uses a truth-set to correct sequencing errors in cell barcodes groupdedup
provides substantial performance improvements over dedup Support SEGMENT read type 3.6.0 Adding tag
and dedup
to CLI 3.5.0 SMRT Link release 11.0 Remove support for CLR data and disable polish
step Enable cluster --use-qvs
as always on 3.4.0 SMRT Link release 10.0.0 Add support for UMI and cell barcode handling, by adding tag
and dedup
Add refine --min-rq
to support RQ filtering for unfiltered <movie>.reads.bam
input 3.3.0 3.2.2 Fix polish
not generating fasta/q output. This bug was introduced in v3.2.0 3.2.1 Fix a gff index 1-off bug in collapse
We have removed implicit dependencies from the bioconda recipe. Please install pbccs
, lima
, and pbcoretools
as needed 3.2.0 polish
dropped support for RS II datasets! Add collapse
step for aligned transcript BAM input Enable CCS-only workflow cluster --use-qvs
Add refine --min-polya-length
Add cluster --singletons
to output unclustered FLNCs; potential sample prep artifacts! Fix minimap2 bugs. Outputs might change slightly 3.1.2 Reduce polish
memory footprint 3.1.1 Edge case fix where polish
would not finish and stale Improve polish
run time for large scale datasets (> 1M CCS) Improve polish
result quality 3.1.0 We outsourced the poly(A) tail removal and concatemer detection into a new tool called refine
. Your custom primers.fasta
is used in this step to detect concatemers THIS WEBSITE AND CONTENT AND ALL SITE-RELATED SERVICES, INCLUDING ANY DATA, ARE PROVIDED "AS IS," WITH ALL FAULTS, WITH NO REPRESENTATIONS OR WARRANTIES OF ANY KIND, EITHER EXPRESS OR IMPLIED, INCLUDING, BUT NOT LIMITED TO, ANY WARRANTIES OF MERCHANTABILITY, SATISFACTORY QUALITY, NON-INFRINGEMENT OR FITNESS FOR A PARTICULAR PURPOSE. YOU ASSUME TOTAL RESPONSIBILITY AND RISK FOR YOUR USE OF THIS SITE, ALL SITE-RELATED SERVICES, AND ANY THIRD PARTY WEBSITES OR APPLICATIONS. NO ORAL OR WRITTEN INFORMATION OR ADVICE SHALL CREATE A WARRANTY OF ANY KIND. ANY REFERENCES TO SPECIFIC PRODUCTS OR SERVICES ON THE WEBSITES DO NOT CONSTITUTE OR IMPLY A RECOMMENDATION OR ENDORSEMENT BY PACIFIC BIOSCIENCES.