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Remove some unecessary changes
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  • subworkflows/local/prepare_genome

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subworkflows/local/prepare_genome/main.nf

Lines changed: 39 additions & 16 deletions
Original file line numberDiff line numberDiff line change
@@ -135,7 +135,7 @@ workflow PREPARE_GENOME {
135135
}
136136

137137
CUSTOM_CATADDITIONALFASTA(
138-
ch_fasta.combine(ch_gtf).map { f, g -> [ [:], f, g ] },
138+
ch_fasta.combine(ch_gtf).map { fasta, gtf -> [ [:], fasta, gtf ] },
139139
ch_add_fasta.map { [ [:], it ] },
140140
gencode ? "gene_type" : featurecounts_group_type
141141
)
@@ -224,11 +224,11 @@ workflow PREPARE_GENOME {
224224
// Build it from scratch if we have FASTA
225225
Channel
226226
.from(file(bbsplit_fasta_list, checkIfExists: true))
227-
.splitCsv()
228-
.flatMap { id, fafile -> [ [ 'id', id ], [ 'fasta', file(fafile, checkIfExists: true) ] ] }
227+
.splitCsv() // Read in 2 column csv file: short_name,path_to_fasta
228+
.flatMap { id, fafile -> [ [ 'id', id ], [ 'fasta', file(fafile, checkIfExists: true) ] ] } // Flatten entries to be able to groupTuple by a common key
229229
.groupTuple()
230-
.map { it -> it[1] }
231-
.collect { [ it ] }
230+
.map { it -> it[1] } // Get rid of keys and keep grouped values
231+
.collect { [ it ] } // Collect entries as a list to pass as "tuple val(short_names), path(path_to_fasta)" to module
232232
.set { ch_bbsplit_fasta_list }
233233

234234
ch_bbsplit_index = BBMAP_BBSPLIT(
@@ -362,6 +362,30 @@ workflow PREPARE_GENOME {
362362
// 14) Salmon index -> can skip genome if transcript_fasta is enough
363363
//------------------------------------------------------
364364
ch_salmon_index = Channel.empty()
365+
//
366+
// Uncompress Salmon index or generate from scratch if required
367+
//
368+
ch_salmon_index = Channel.empty()
369+
if (salmon_index) {
370+
if (salmon_index.endsWith('.tar.gz')) {
371+
ch_salmon_index = UNTAR_SALMON_INDEX ( [ [:], salmon_index ] ).untar.map { it[1] }
372+
ch_versions = ch_versions.mix(UNTAR_SALMON_INDEX.out.versions)
373+
} else {
374+
ch_salmon_index = Channel.value(file(salmon_index))
375+
}
376+
} else if ('salmon' in prepare_tool_indices) {
377+
if (ch_transcript_fasta && fasta_provided) {
378+
// build from transcript FASTA + genome FASTA
379+
ch_salmon_index = SALMON_INDEX(ch_fasta, ch_transcript_fasta).index
380+
ch_versions = ch_versions.mix(SALMON_INDEX.out.versions)
381+
}
382+
else if (ch_transcript_fasta) {
383+
// some Salmon module can run with just a transcript FASTA
384+
ch_salmon_index = SALMON_INDEX([], ch_transcript_fasta).index
385+
ch_versions = ch_versions.mix(SALMON_INDEX.out.versions)
386+
}
387+
}
388+
365389
if ('salmon' in prepare_tool_indices) {
366390
if (salmon_index) {
367391
// use user-provided salmon index
@@ -388,18 +412,17 @@ workflow PREPARE_GENOME {
388412
// 15) Kallisto index -> only needs transcript FASTA
389413
//--------------------------------------------------
390414
ch_kallisto_index = Channel.empty()
391-
if ('kallisto' in prepare_tool_indices) {
392-
if (kallisto_index) {
393-
if (kallisto_index.endsWith('.tar.gz')) {
394-
ch_kallisto_index = UNTAR_KALLISTO_INDEX ([ [:], file(kallisto_index, checkIfExists: true) ]).untar
395-
ch_versions = ch_versions.mix(UNTAR_KALLISTO_INDEX.out.versions)
396-
} else {
397-
ch_kallisto_index = Channel.value([ [:], file(kallisto_index, checkIfExists: true) ])
398-
}
415+
if (kallisto_index) {
416+
if (kallisto_index.endsWith('.tar.gz')) {
417+
ch_kallisto_index = UNTAR_KALLISTO_INDEX ( [ [:], kallisto_index ] ).untar
418+
ch_versions = ch_versions.mix(UNTAR_KALLISTO_INDEX.out.versions)
419+
} else {
420+
ch_kallisto_index = Channel.value([[:], file(kallisto_index)])
399421
}
400-
else if (ch_transcript_fasta) {
401-
ch_kallisto_index = KALLISTO_INDEX(ch_transcript_fasta.map { [ [:], it ] }).index
402-
ch_versions = ch_versions.mix(KALLISTO_INDEX.out.versions)
422+
} else {
423+
if ('kallisto' in prepare_tool_indices) {
424+
ch_kallisto_index = KALLISTO_INDEX ( ch_transcript_fasta.map { [ [:], it] } ).index
425+
ch_versions = ch_versions.mix(KALLISTO_INDEX.out.versions)
403426
}
404427
}
405428

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