Available Modules
Modules are the building stones of all DSL2 nf-core blocks. You can find more info from nf-core website, if you would like to write your own module.
- bam 170
- fasta 166
- vcf 120
- fastq 117
- genomics 114
- metagenomics 79
- genome 71
- index 70
- reference 65
- alignment 62
- gatk4 61
- bed 60
- assembly 59
- cram 56
- sam 49
- sort 48
- variant calling 38
- annotation 38
- structural variants 38
- align 37
- database 34
- merge 32
- filter 31
- gff 28
- bacteria 28
- map 28
- statistics 27
- coverage 26
- variants 24
- qc 23
- quality control 22
- gtf 21
- classify 21
- nanopore 20
- download 20
- cnv 20
- taxonomic profiling 18
- k-mer 18
- gfa 18
- variant 18
- split 18
- contamination 18
- pacbio 17
- sentieon 17
- classification 16
- taxonomy 16
- MSA 16
- binning 15
- somatic 15
- count 15
- quality 15
- convert 15
- clustering 14
- ancient DNA 14
- copy number 14
- proteomics 14
- VCF 14
- contigs 13
- phylogeny 13
- single-cell 13
- imputation 13
- bedtools 13
- conversion 13
- graph 12
- gvcf 12
- bisulfite 12
- sv 12
- trimming 12
- reporting 12
- isoseq 12
- variation graph 12
- bcftools 12
- methylseq 11
- picard 11
- cna 11
- rnaseq 11
- methylation 11
- protein 11
- bisulphite 11
- databases 11
- build 11
- illumina 11
- QC 11
- consensus 11
- bqsr 11
- compression 11
- table 11
- sequences 10
- phage 10
- 5mC 10
- imaging 10
- metrics 10
- antimicrobial resistance 10
- kmer 10
- long-read 10
- expression 10
- stats 10
- serotype 10
- visualisation 10
- indexing 10
- tsv 10
- matrix 9
- searching 9
- openms 9
- depth 9
- cluster 9
- markduplicates 9
- plot 9
- bins 9
- base quality score recalibration 9
- amr 9
- protein sequence 9
- histogram 9
- neural network 9
- DNA methylation 9
- scWGBS 9
- WGBS 9
- wgs 9
- aDNA 9
- haplotype 9
- pairs 9
- demultiplex 9
- pangenome graph 9
- metagenome 8
- mappability 8
- completeness 8
- annotate 8
- bwa 8
- virus 8
- LAST 8
- checkm 8
- db 8
- damage 8
- aligner 8
- mmseqs2 8
- genotype 8
- samtools 8
- archaeogenomics 8
- palaeogenomics 8
- validation 8
- cooler 8
- transcript 8
- biscuit 8
- iCLIP 8
- bcf 8
- low-coverage 8
- machine learning 8
- bisulfite sequencing 8
- plink 8
- filtering 8
- repeat 8
- segmentation 7
- bismark 7
- spatial 7
- transcriptome 7
- kraken2 7
- blast 7
- phasing 7
- peaks 7
- glimpse 7
- decompression 7
- hmmsearch 7
- structure 7
- population genetics 7
- gff3 7
- gene 7
- ucsc 7
- dedup 7
- search 7
- mags 7
- complexity 7
- newick 7
- umi 7
- long reads 7
- sequence 7
- germline 7
- ncbi 7
- mkref 7
- evaluation 7
- mag 7
- seqkit 7
- differential 7
- example 7
- duplicates 6
- prokaryote 6
- hmmer 6
- mitochondria 6
- snp 6
- json 6
- single 6
- NCBI 6
- demultiplexing 6
- antimicrobial resistance genes 6
- bedGraph 6
- deduplication 6
- feature 6
- tumor-only 6
- cnvkit 6
- mapping 6
- vsearch 6
- gzip 6
- plasmid 6
- short-read 6
- pangenome 6
- mirna 6
- antimicrobial peptides 6
- low frequency variant calling 6
- genotyping 6
- prediction 6
- kmers 6
- scRNA-seq 6
- riboseq 5
- counts 5
- mutect2 5
- arg 5
- enrichment 5
- de novo 5
- csv 5
- adapters 5
- text 5
- isolates 5
- mem 5
- report 5
- single cell 5
- multiple sequence alignment 5
- fragment 5
- call 5
- 3-letter genome 5
- interval 5
- antibiotic resistance 5
- deamination 5
- splicing 5
- query 5
- de novo assembly 5
- amps 5
- MAF 5
- detection 5
- clipping 5
- svtk 5
- summary 5
- kallisto 5
- microbiome 5
- mpileup 5
- view 5
- benchmark 5
- extract 5
- idXML 5
- visualization 5
- diversity 5
- msa 5
- sourmash 5
- family 4
- DNA sequencing 4
- quantification 4
- palaeogenetics 4
- ampir 4
- hic 4
- chunk 4
- paf 4
- containment 4
- interval_list 4
- bgzip 4
- fungi 4
- diamond 4
- haplotypecaller 4
- bcl2fastq 4
- reference-free 4
- resistance 4
- ancestry 4
- umitools 4
- ngscheckmate 4
- read depth 4
- malt 4
- copy number alteration calling 4
- merging 4
- phylogenetic placement 4
- STR 4
- public datasets 4
- ATAC-seq 4
- ont 4
- microsatellite 4
- taxonomic classification 4
- CLIP 4
- fgbio 4
- SV 4
- circrna 4
- hybrid capture sequencing 4
- genome assembler 4
- cut 4
- ganon 4
- indels 4
- profiling 4
- targeted sequencing 4
- retrotransposon 4
- sequencing 4
- matching 4
- logratio 4
- DNA sequence 4
- compare 4
- structural 4
- BGC 4
- deep learning 4
- ccs 4
- fastx 4
- archaeogenetics 4
- tabular 4
- bin 4
- propr 4
- hmmcopy 4
- HiFi 4
- xeniumranger 4
- FASTQ 4
- happy 4
- isomir 4
- miscoding lesions 4
- redundancy 4
- biosynthetic gene cluster 4
- compress 4
- profile 4
- genmod 4
- telomere 4
- bigwig 4
- concatenate 4
- ranking 4
- bedgraph 4
- parsing 4
- microarray 4
- normalization 4
- peak-calling 4
- sample 4
- add 4
- insert 3
- das_tool 3
- typing 3
- informative sites 3
- observations 3
- lossless 3
- bacterial 3
- PCA 3
- tabix 3
- pairsam 3
- deeparg 3
- structural_variants 3
- identity 3
- snps 3
- scores 3
- relatedness 3
- kinship 3
- fingerprint 3
- survivor 3
- plink2 3
- genomes 3
- mtDNA 3
- bim 3
- fam 3
- replace 3
- pan-genome 3
- spaceranger 3
- entrez 3
- mzml 3
- prokka 3
- rsem 3
- preprocessing 3
- duplication 3
- score 3
- mapper 3
- html 3
- organelle 3
- krona 3
- genome assembly 3
- transcripts 3
- pseudoalignment 3
- krona chart 3
- reports 3
- windowmasker 3
- notebook 3
- amplicon sequencing 3
- variant_calling 3
- dna 3
- cfDNA 3
- HMM 3
- ligate 3
- PacBio 3
- gridss 3
- chimeras 3
- gatk4spark 3
- npz 3
- transposons 3
- uLTRA 3
- SNP 3
- minimap2 3
- genotype-based deconvoltion 3
- popscle 3
- long_read 3
- fastk 3
- reads 3
- untar 3
- UMI 3
- uncompress 3
- mlst 3
- subsample 3
- unzip 3
- wxs 3
- wastewater 3
- zip 3
- archiving 3
- polishing 3
- shapeit 3
- vrhyme 3
- spark 3
- benchmarking 3
- dictionary 3
- amplicon sequences 3
- small indels 3
- panel 3
- indel 3
- ambient RNA removal 3
- das tool 3
- clean 3
- adapter trimming 3
- atac-seq 3
- chip-seq 3
- pileup 3
- bamtools 3
- wig 3
- png 3
- rna 3
- host 3
- bakta 3
- checkv 3
- highly_multiplexed_imaging 3
- mcmicro 3
- image_analysis 3
- ataqv 3
- arriba 3
- fusion 3
- eukaryotes 3
- prokaryotes 3
- genome mining 3
- cut up 3
- quality trimming 3
- remove 3
- angsd 3
- chromosome 3
- bwameth 3
- aln 3
- abundance 3
- bracken 3
- combine 3
- comparisons 3
- cat 3
- nucleotide 3
- image 3
- mkfastq 3
- microbes 3
- fai 3
- cellranger 3
- intervals 3
- converter 3
- gene expression 3
- C to T 3
- roh 3
- pypgx 3
- complement 3
- kraken 3
- cool 3
- hi-c 3
- gsea 3
- rna_structure 3
- repeat expansion 3
- neubi 3
- RNA 3
- amplify 3
- fcs-gx 3
- macrel 3
- prefetch 3
- virulence 3
- DRAMP 3
- CRISPR 3
- dump 3
- polyA_tail 2
- comparison 2
- proportionality 2
- screening 2
- ichorcna 2
- junctions 2
- mitochondrion 2
- salmonella 2
- rtgtools 2
- image_processing 2
- maximum likelihood 2
- iphop 2
- registration 2
- gwas 2
- refine 2
- preseq 2
- reheader 2
- krakentools 2
- concat 2
- Pharmacogenetics 2
- interactive 2
- allele 2
- rename 2
- krakenuniq 2
- tbi 2
- intersect 2
- SimpleAF 2
- scatter 2
- union 2
- screen 2
- khmer 2
- bustools 2
- seqtk 2
- normalize 2
- guide tree 2
- norm 2
- hidden Markov model 2
- cleaning 2
- hlala_typing 2
- cnvnator 2
- transcriptomic 2
- collate 2
- gene set analysis 2
- ome-tif 2
- orthology 2
- parallelized 2
- awk 2
- phase 2
- concordance 2
- BAM 2
- bedpe 2
- blastn 2
- repeats 2
- mudskipper 2
- dict 2
- fixmate 2
- proteome 2
- soft-clipped clusters 2
- ChIP-seq 2
- trgt 2
- gene set 2
- bam2fq 2
- nucleotides 2
- rgfa 2
- mask 2
- mapcounter 2
- hla_typing 2
- hlala 2
- hla 2
- intersection 2
- windows 2
- scaffolding 2
- tnhaplotyper2 2
- MCMICRO 2
- smrnaseq 2
- RNA sequencing 2
- somatic variants 2
- varcal 2
- mirdeep2 2
- fusions 2
- trancriptome 2
- tama 2
- gstama 2
- pair 2
- serogroup 2
- sketch 2
- aggregate 2
- signature 2
- ped 2
- small genome 2
- de novo assembler 2
- RNA-Seq 2
- GPU-accelerated 2
- simulate 2
- artic 2
- svdb 2
- read-group 2
- demultiplexed reads 2
- standardization 2
- ancient dna 2
- taxonomic profile 2
- standardise 2
- standardisation 2
- otu tables 2
- taxon tables 2
- FracMinHash sketch 2
- antismash 2
- anndata 2
- bfiles 2
- adapter 2
- import 2
- edit distance 2
- library 2
- HOPS 2
- variant pruning 2
- gene labels 2
- shigella 2
- secondary metabolites 2
- MaltExtract 2
- switch 2
- effect prediction 2
- snpeff 2
- snpsift 2
- cancer genomics 2
- join 2
- NRPS 2
- RiPP 2
- antibiotics 2
- graph layout 2
- nextclade 2
- primer 2
- long-read sequencing 2
- checksum 2
- link 2
- tree 2
- contig 2
- trim 2
- minhash 2
- mash 2
- sequence analysis 2
- scaffold 2
- megan 2
- distance 2
- frame-shift correction 2
- polish 2
- runs_of_homozygosity 2
- lofreq 2
- authentication 2
- barcode 2
- transformation 2
- vg 2
- vcflib 2
- removal 2
- purge duplications 2
- doublets 2
- msisensor-pro 2
- micro-satellite-scan 2
- tumor 2
- msi 2
- instability 2
- MSI 2
- homoploymer 2
- Streptococcus pneumoniae 2
- GC content 2
- Duplication purging 2
- Read depth 2
- xenograft 2
- spatial_transcriptomics 2
- duplicate 2
- resolve_bioscience 2
- genomad 2
- graft 2
- sequenzautils 2
- profiles 2
- instrain 2
- interval list 2
- joint genotyping 2
- eido 2
- expansionhunterdenovo 2
- regression 2
- interactions 2
- salmon 2
- lift 2
- metamaps 2
- deconvolution 2
- bayesian 2
- gatk 2
- format 2
- transcriptomics 2
- identifier 2
- calling 2
- metagenomic 2
- blastp 2
- deseq2 2
- rna-seq 2
- estimation 2
- immunoprofiling 2
- amptransformer 2
- repeat_expansions 2
- samplesheet 2
- long terminal retrotransposon 2
- cnv calling 2
- zlib 2
- filtermutectcalls 2
- allele-specific 2
- orf 2
- tab 2
- single cells 2
- genome bins 2
- emboss 2
- dereplicate 2
- realignment 2
- unaligned 2
- validate 2
- CNV 2
- evidence 2
- vdj 2
- metadata 2
- panelofnormals 2
- microbial 2
- eigenstrat 2
- variation 2
- cvnkit 2
- leviosam2 2
- correction 2
- ampgram 2
- bloom filter 2
- settings 2
- GEO 2
- regions 2
- merge mate pairs 2
- baf 2
- parse 2
- short reads 2
- spatial_omics 2
- fetch 2
- function 2
- random forest 2
- xz 2
- sra-tools 2
- k-mer index 2
- COBS 2
- archive 2
- metagenomes 2
- pharokka 2
- fasterq-dump 2
- reads merging 2
- long terminal repeat 2
- eCLIP 2
- duplex 2
- retrotransposons 2
- UMIs 2
- gem 2
- heatmap 2
- structural-variant calling 2
- recombination 2
- taxids 1
- nuclear segmentation 1
- sccmec 1
- emoji 1
- taxon name 1
- circular 1
- variantcalling 1
- spot 1
- umicollapse 1
- tag 1
- extraction 1
- ribosomal RNA 1
- streptococcus 1
- signatures 1
- spatype 1
- realign 1
- quality_control 1
- scvi 1
- scRNA-Seq 1
- cell_barcodes 1
- orthogroup 1
- solo 1
- fracminhash sketch 1
- hash sketch 1
- import segmentation 1
- quality check 1
- spa 1
- go 1
- coptr 1
- featuretable 1
- genepred 1
- bedtobigbed 1
- bigbed 1
- bedgraphtobigwig 1
- mass spectrometry 1
- Mycobacterium tuberculosis 1
- chromosomal rearrangements 1
- eucaryotes 1
- fast5 1
- coding 1
- logFC 1
- differential expression 1
- subsetting 1
- mygene 1
- cds 1
- transcroder 1
- sage 1
- polya tail 1
- detecting svs 1
- barcodes 1
- ptr 1
- short-read sequencing 1
- sequencing adapters 1
- doublet_detection 1
- svtk/baftest 1
- baftest 1
- countsvtypes 1
- rdtest2vcf 1
- p-value 1
- rdtest 1
- pile up 1
- ucsc/liftover 1
- gtftogenepred 1
- refflat 1
- orthologs 1
- vcf2bed 1
- decompress 1
- homology 1
- paired reads merging 1
- rRNA 1
- pseudodiploid 1
- guidetree 1
- interleave 1
- droplet based single cells 1
- header 1
- human removal 1
- seq 1
- busco 1
- selection 1
- random draw 1
- pseudohaploid 1
- bwamem2 1
- sertotype 1
- bwameme 1
- grabix 1
- freqsum 1
- ribosomal 1
- 10x 1
- bam2seqz 1
- gc_wiggle 1
- induce 1
- retrieval 1
- sex determination 1
- Pacbio 1
- metagenome assembler 1
- relative coverage 1
- cut&run 1
- cellsnp 1
- scramble 1
- trimfq 1
- cluster analysis 1
- donor deconvolution 1
- genotype-based demultiplexing 1
- clusteridentifier 1
- vcflib/vcffixup 1
- peak-caller 1
- cut&tag 1
- chromatin 1
- sequence headers 1
- seacr 1
- assembly-binning 1
- scanpy 1
- applyvarcal 1
- VQSR 1
- variant recalibration 1
- AC/NS/AF 1
- subseq 1
- grep 1
- lexogen 1
- genetic sex 1
- regulatory network 1
- nanopore sequencing 1
- dist 1
- CRAM 1
- relabel 1
- SMN1 1
- SMN2 1
- cell segmentation 1
- translation 1
- POA 1
- sniffles 1
- core 1
- snippy 1
- cram-size 1
- overlap-based merging 1
- grea 1
- size 1
- dbnsfp 1
- predictions 1
- extension 1
- SNPs 1
- invariant 1
- constant 1
- cobra 1
- rna velocity 1
- selector 1
- paraphase 1
- transposable element 1
- longread 1
- generic 1
- rare variants 1
- decontamination 1
- hostile 1
- coreutils 1
- error 1
- morphology 1
- gnu 1
- transcription factors 1
- de-novo 1
- sha256 1
- check 1
- 256 bit 1
- hashing-based deconvoltion 1
- hamming-distance 1
- shinyngs 1
- exploratory 1
- boxplot 1
- density 1
- features 1
- resegment 1
- sliding window 1
- source tracking 1
- downsample bam 1
- prior knowledge 1
- search engine 1
- python 1
- quarto 1
- reverse complement 1
- variant-calling 1
- simulation 1
- standardize 1
- hmmfetch 1
- poolseq 1
- dbsnp 1
- parser 1
- parquet 1
- stardist 1
- mgf 1
- decompose 1
- multiallelic 1
- raw 1
- mass_error 1
- small variants 1
- transmembrane 1
- resistance genes 1
- genome graph 1
- tnseq 1
- resfinder 1
- r 1
- uniques 1
- multiqc 1
- chloroplast 1
- ATACseq 1
- nucleotide sequence 1
- fastqfilter 1
- distance-based 1
- minimum_evolution 1
- vsearch/fastqfilter 1
- groupby 1
- phylogenetics 1
- tnscope 1
- bgen 1
- confidence 1
- Read coverage histogram 1
- blat 1
- alr 1
- clr 1
- vsearch/dereplicate 1
- boxcox 1
- assay 1
- corpcor 1
- telseq 1
- Escherichia coli 1
- correlation 1
- coexpression 1
- decoy 1
- htseq 1
- shift 1
- spectral clustering 1
- standard 1
- svg 1
- xml 1
- gost 1
- idx 1
- mutect 1
- deep variant 1
- rad 1
- script 1
- comparative genomics 1
- sequence similarity 1
- gprofiler2 1
- tags 1
- structural variant 1
- bam2fastx 1
- bam2fastq 1
- immcantation 1
- airrseq 1
- java 1
- rank 1
- immunoinformatics 1
- co-orthology 1
- hashing-based deconvolution 1
- impute-info 1
- vector 1
- rrna 1
- parallel 1
- microRNA 1
- sompy 1
- miRNA 1
- Illumina 1
- kma 1
- reformatting 1
- plastid 1
- peak picking 1
- Staging 1
- site frequency spectrum 1
- ancestral alleles 1
- functional 1
- cytosure 1
- derived alleles 1
- tnfilter 1
- staging 1
- genotypegvcf 1
- joint-genotyping 1
- install 1
- introns 1
- haplotag 1
- gaps 1
- transform 1
- array_cgh 1
- homologs 1
- dnascope 1
- cgMLST 1
- case/control 1
- spatial_neighborhoods 1
- VCFtools 1
- verifybamid 1
- DNA contamination estimation 1
- associations 1
- genetics 1
- construct 1
- WGS 1
- graph projection to vcf 1
- AT content 1
- GWAS 1
- uniq 1
- nucBed 1
- bclconvert 1
- extractunbinned 1
- redundant 1
- linkbins 1
- association 1
- refresh 1
- sintax 1
- clahe 1
- vsearch/sort 1
- usearch 1
- deduplicate 1
- vcfbreakmulti 1
- pangenome-scale 1
- uniparental 1
- controlstatistics 1
- pharmacogenetics 1
- elprep 1
- files 1
- elfasta 1
- functional analysis 1
- biological activity 1
- omics 1
- structural-variants 1
- upd 1
- disomy 1
- nucleotide content 1
- snv 1
- downsample 1
- tag2tag 1
- subsample bam 1
- vcf2db 1
- gemini 1
- maf 1
- lua 1
- toml 1
- Bayesian 1
- scimap 1
- long read alignment 1
- targz 1
- dnamodelapply 1
- hwe statistics 1
- liftover 1
- readproteingroups 1
- collapse 1
- genotype likelihood 1
- eigenvectors 1
- hicPCA 1
- sliding 1
- reference-independent 1
- hwe equilibrium 1
- snakemake 1
- workflow 1
- seqfu 1
- hardy-weinberg 1
- workflow_mode 1
- Read report 1
- predict 1
- drug categorization 1
- multi-tool 1
- ATACshift 1
- createreadcountpanelofnormals 1
- copyratios 1
- denoisereadcounts 1
- readwriter 1
- probabilistic realignment 1
- n50 1
- tarball 1
- cell_phenotyping 1
- all versus all 1
- cell_type_identification 1
- wavefront 1
- whamg 1
- wham 1
- tar 1
- copy-number 1
- copy number analysis 1
- gender determination 1
- machine_learning 1
- translate 1
- jvarkit 1
- proteus 1
- copy number alterations 1
- nanoq 1
- Read filters 1
- copy number variation 1
- yahs 1
- geo 1
- setgt 1
- mapad 1
- adna 1
- c to t 1
- Read trimming 1
- mashmap 1
- lofreq/call 1
- readgroup 1
- gene-calling 1
- zipperbams 1
- single molecule 1
- generate 1
- random 1
- lint 1
- fq 1
- rust 1
- variant caller 1
- somatic variant calling 1
- germline variant calling 1
- bacterial variant calling 1
- bootstrapping 1
- UShER 1
- gamma 1
- gangstr 1
- unmapped 1
- heattree 1
- targets 1
- annotateintervals 1
- variant quality score recalibration 1
- vqsr 1
- asereadcounter 1
- bedtointervallist 1
- calculatecontamination 1
- cross-samplecontamination 1
- getpileupsummaries 1
- calibratedragstrmodel 1
- cnnscorevariants 1
- collectreadcounts 1
- collectsvevidence 1
- ubam 1
- groupreads 1
- short variant discovery 1
- embl 1
- blastx 1
- segment 1
- duphold 1
- structural variation 1
- depth information 1
- escherichia coli 1
- PEP 1
- schema 1
- pep 1
- eigenstratdatabasetools 1
- eklipse 1
- circos 1
- deletion 1
- split by chromosome 1
- genbank 1
- duplexumi 1
- swissprot 1
- Streptococcus pyogenes 1
- endogenous DNA 1
- percent on target 1
- cache 1
- str 1
- faqcs 1
- antibiotic resistance genes 1
- ARGs 1
- ANI 1
- SRA 1
- ENA 1
- public 1
- consensus sequence 1
- combinegvcfs 1
- composestrtablefile 1
- scatterplot 1
- genome profile 1
- shiftfasta 1
- shiftintervals 1
- site depth 1
- splitcram 1
- splitintervals 1
- svannotate 1
- svcluster 1
- variantfiltration 1
- recalibration model 1
- variantrecalibrator 1
- gawk 1
- txt 1
- file parsing 1
- bgc 1
- compound 1
- selectvariants 1
- models 1
- genome size 1
- genome heterozygosity 1
- repeat content 1
- Salmonella Typhi 1
- Mykrobe 1
- gfastats 1
- genome summary 1
- genome manipulation 1
- genome statistics 1
- gget 1
- low coverage 1
- Sample 1
- Haplotypes 1
- shiftchain 1
- revert 1
- dragstr 1
- germline contig ploidy 1
- condensedepthevidence 1
- createsequencedictionary 1
- createsomaticpanelofnormals 1
- determinegermlinecontigploidy 1
- duplication metrics 1
- estimatelibrarycomplexity 1
- filterintervals 1
- filtervarianttranches 1
- tranche filtering 1
- gatherbqsrreports 1
- genomicsdb 1
- genomicsdbimport 1
- jointgenotyping 1
- panelofnormalscreation 1
- germlinecnvcaller 1
- reblockgvcf 1
- germlinevariantsites 1
- getpileupsumaries 1
- readcountssummary 1
- indexfeaturefile 1
- learnreadorientationmodel 1
- readorientationartifacts 1
- leftalignandtrimvariants 1
- mergebamalignment 1
- mutectstats 1
- snvs 1
- postprocessgermlinecnvcalls 1
- preprocessintervals 1
- printreads 1
- printsvevidence 1
- cumulative coverage 1
- corrrelation 1
- joint-variant-calling 1
- smaller fastqs 1
- temperate 1
- virulent 1
- bacphlip 1
- mouse 1
- bamtools/convert 1
- yaml 1
- bamtools/split 1
- bamUtil 1
- trimBam 1
- element 1
- illumiation_correction 1
- background_correction 1
- microscopy 1
- clumping fastqs 1
- deduping 1
- autofluorescence 1
- csi 1
- BCF 1
- update header 1
- biallelic 1
- homozygosity 1
- autozygosity 1
- sorting 1
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- metagenome-assembled genomes 1
- mass-spectroscopy 1
- mcr-1 1
- MD5 1
- 128 bit 1
- plotting 1
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