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Releases: nf-core/sarek

Sarek 3.2.2 - Vuoinesluobbalah

15 Jun 14:24
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Sarek 3.2.1 - Pierikjaure

08 Jun 12:53
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Sarek 3.2.0 - Bierikjávrre

05 Jun 11:31
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Full Changelog: 3.1.2...3.2.0

Sarek 3.1.2 - Lesser Lule River

05 Jan 18:06
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Sarek 3.1.1 - Lilla Luleälven

21 Nov 13:32
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Sarek 3.1 - Rapaätno

16 Nov 13:30
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Sarek 3.0.2 - Lájtávrre

26 Sep 19:07
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Sarek 3.0.1 - Saiva

18 Aug 11:48
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Sarek 3.0 - Skierfe

21 Jul 11:34
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  • Porting to DSL2
  • Use CRAM files where possible
  • Add new tools: DragMap, DeepVariant, Joint germline calling, Haplotypecaller single sample, CNVKit Somatic, Tiddit Somatic
  • Replaced tools: Trimgalore -> Fastp, Qualimap -> Mosdepth
  • New references: BWAMem2, DragMap, Germline Resource
  • Add a new entry --step markduplicates
  • Steps can be started from bam or cram files
  • Added --paired_variant_calling_only to skip normal computations for paired samples
  • Only unmatched tumor samples will be run in single mode
  • Input fastq files are split by default and mapped in parallel
  • Bam2Fastq: changed to using samtools
  • Samplesheet is now in CSV format with a header line with improved validation and flexibility
  • New parameter --skip_tools retires --skip_qc, --skip_markduplicates and --skip_bqsr
  • --sequencing_center renamed to --seq_platform`
  • New parameter --wes must be set for targeted data
  • New parameter --save_bam_ouput to store results file in BAM format instead of CRAM
  • Additional VEP output formats
  • Additional VEP plugins: loftee, spliceAI, spliceRegions, dbnsfp
  • Remove sentieon support

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Full Changelog: 2.7.2...3.0

Sarek 2.7.2 - Áhkká

10 Jun 09:45
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