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TRANSVIHMI
nfernandez
GeVarLi
Commits
6c2b7b7a
Commit
6c2b7b7a
authored
1 year ago
by
nicolas.fernandez_ird.fr
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2023-04 release
parent
ec95cbd2
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README.md
+41
-42
41 additions, 42 deletions
README.md
Start_GeVarLi.sh
+2
-2
2 additions, 2 deletions
Start_GeVarLi.sh
configuration/config.yaml
+3
-3
3 additions, 3 deletions
configuration/config.yaml
with
46 additions
and
47 deletions
README.md
+
41
−
42
View file @
6c2b7b7a
# GeVarLi: GEnome assembly, VARiant calling and LIneage assignation #

 | Catalina (10.15.7) | Big Sure (11.6.3) | Monterey (12.6.0) | Ventura (13.
2
.1)/E6055C?icon=apple&label&list=|&scale=0.9
>
)
 | Catalina (10.15.7) | Big Sure (11.6.3) | Monterey (12.6.0) | Ventura (13.
3
.1)/E6055C?icon=apple&label&list=|&scale=0.9
>
)
 | Focal Fossa (20.04) | Jammy Jellyfish (22.04)/772953?icon=https://www.svgrepo.com/show/25424/ubuntu-logo.svg&label&list=|&scale=0.9
>
)
 | Focal Fossa (20.04) | Jammy Jellyfish (22.04)/00BCF2?icon=windows&label&list=|&scale=0.9
>
)

...
...
@@ -12,9 +12,9 @@









## ~ ABOUT ~ ##
...
...
@@ -41,20 +41,19 @@ The Covid-19 epidemic has highlighted the disparities that remain between contin
-
Sickle-trim (_quality trimming_)
-
Reads mapping
-
(_bam files_)
-
-
-
Variants calling
-
(_vcf files_)
-
(_bed files_)
-
Visualization (IGV)
-
Variants calling and filtering (_vcf files_)
-
Genome coverage (_statistics reports_)
-
Consensus sequences (_fasta file_)
-
Genomes classification
-
Nextclade
-
Pangolin
-
Nextclade
(_consensus quality and lineages reports_)
-
Pangolin
(_lineages reports_)
### Version ###
*V.2023.0
3
*
*V.2023.0
4
*
### Rulegraph ###
...
...
@@ -189,8 +188,8 @@ _Option-2: Edit **fastq-screen.conf** file in **./configuration/** directory_
First run will auto-created _(only once)_:
-
Snakemake-Base conda environment _(Snakemake, Mamba, Rename, GraphViz)_
-
GeVarLi-conda environments _(tools used by GeVarLi)_
-
Indexes for BWA and BOWTIE2 aligners _(for each fasta genomes in resources)_
-
GeVarLi-
Tools
conda environments _(tools used by GeVarLi)_
-
Indexes for BWA and BOWTIE2 aligners _(for each fasta genomes in resources
/ directory
)_
_This may take some time, depending on your internet connection and your computer_
...
...
@@ -205,10 +204,10 @@ _Some [temp] tagged files are removed by default, to save disk usage_
├── 📂 archives/
│ └── 📦 Results_
{
YYYY-MM-DD_HHhMM
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_
{
SAMPLES
}
_archive.tar.gz
└── 📂 results/
├── 🧬 All_consensus_sequences.fasta
├── 📊 All_genome_coverages.tsv
├── 📊 All_nextclade_lineages.tsv
├── 📊 All_pangolin_lineages.tsv
├── 🧬 All_
{
REFERENCE
}
_
consensus_sequences.fasta
├── 📊 All_
{
REFERENCE
}
_
genome_coverages.tsv
├── 📊 All_
{
REFERENCE
}
_
nextclade_lineages.tsv
├── 📊 All_
{
REFERENCE
}
_
pangolin_lineages.tsv
├── 🌐 All_readsQC_reports.html
├── 📂 00_Quality_Control/
│ ├── 📂 fastq-screen/
...
...
@@ -229,40 +228,40 @@ _Some [temp] tagged files are removed by default, to save disk usage_
│ ├── 📄 multiqc_general_stats.txt
| └── 📄 multiqc_sources.txt
├── 📂 01_Trimmidapt
│ ├── 📂 cutad
{
SAMPLE
}
_cutadapt-removed_R
{
1/2
}
.fastq.gz
# [temp]
│ │ └── 📦
{
S
│ ├── 📂 cutad
apt/
│ │ └── 📦
{
S
AMPLE
}
_cutadapt-removed_R
{
1/2
}
.fastq.gz
# [temp]
│ └── 📂 sickle/
│ ├── 📦
{
SAMPLE
}
_sickle-trimmed_R
{
1/2
}
.fastq.gz
# [temp]
│ └── 📦
{
SAMPLE
}
_sickle-trimmed_SE.fastq.gz
# [temp]
├── 📂 02_Mapping/
│ ├── 🧭
{
SAMPLE
}
_
{
ALIGNER
}
_mark-dup.bam
│ ├── 🗂️
{
SAMPLE
}
_
{
ALIGNER
}
_mark-dup.bam.bai
│ ├── 🧭
{
SAMPLE
}
_
{
ALIGNER
}
_mark-dup.primerclipped.bam
│ ├── 🗂️
{
SAMPLE
}
_
{
ALIGNER
}
_mark-dup.primerclipped.bam.bai
│ ├── 🧭
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_mark-dup.bam
│ ├── 🗂️
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_mark-dup.bam.bai
│ ├── 🧭
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_mark-dup.primerclipped.bam
│ ├── 🗂️
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_mark-dup.primerclipped.bam.bai
│ ├── 🧭
{
SAMPLE
}
_
{
ALIGNER
}
-mapped
.sam
# [temp]
│ ├── 🧭
{
SAMPLE
}
_
{
ALIGNER
}
_sorted-by-names.bam
# [temp]
│ ├── 🧭
{
SAMPLE
}
_
{
ALIGNER
}
_fixed-mate.bam
# [temp]
│ └── 🧭
{
SAMPLE
}
_
{
ALIGNER
}
_sorted.bam
# [temp]
│ ├── 🧭
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_sorted-by-names.bam
# [temp]
│ ├── 🧭
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_fixed-mate.bam
# [temp]
│ └── 🧭
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_sorted.bam
# [temp]
├── 📂 03_Coverage/
│ ├── 📊
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_coverage-stats.tsv
│ ├── 🛏️
{
SAMPLE
}
_
{
ALIGNER
}
_genome-cov.bed
# [temp]
│ ├── 🛏️
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_min-cov-filt.bed
# [temp]
│ └── 🛏️
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_low-cov-mask.bed
# [temp]
│ ├── 📊
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_coverage-stats.tsv
│ ├── 🛏️
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_genome-cov.bed
# [temp]
│ ├── 🛏️
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_min-cov-filt.bed
# [temp]
│ └── 🛏️
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_low-cov-mask.bed
# [temp]
├── 📂 04_Variants/
│ ├── 🧬
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_masked-ref.fasta
│ ├── 🗂️
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_masked-ref.fasta.fai
│ ├── 🧭
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_indel-qual.bam
│ ├── 🗂️
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_indel-qual.bai
│ ├── 🧮️
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_variant-call.vcf
│ ├── 🧮️
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_variant-filt.vcf
│ ├── 📦
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_variant-filt.vcf.bgz
# [temp]
│ └── 🗂️
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_variant-filt.vcf.bgz.tbi
# [temp]
│ ├── 🧬
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_masked-ref.fasta
│ ├── 🗂️
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_masked-ref.fasta.fai
│ ├── 🧭
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_indel-qual.bam
│ ├── 🗂️
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_indel-qual.bai
│ ├── 🧮️
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_variant-call.vcf
│ ├── 🧮️
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_variant-filt.vcf
│ ├── 📦
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_variant-filt.vcf.bgz
# [temp]
│ └── 🗂️
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_variant-filt.vcf.bgz.tbi
# [temp]
├── 📂 05_Consensus/
│ └── 🧬
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_consensus.fasta
│ └── 🧬
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_consensus.fasta
├── 📂 06_Lineages/
│ ├── 📊
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_nextclade-report.tsv
│ ├── 📊
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_pangolin-report.csv
│ └── 📂
{
SAMPLE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_nextclade-all/
│ ├── 📊
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_nextclade-report.tsv
│ ├── 📊
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_pangolin-report.csv
│ └── 📂
{
SAMPLE
}
_
{
REFERENCE
}
_
{
ALIGNER
}
_
{
MINCOV
}
_nextclade-all/
│ ├── 🧬 nextclade.aligned.fasta
│ ├── 📊 nextclade.csv
│ ├── 📊 nextclade.errors.csv
...
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Start_GeVarLi.sh
+
2
−
2
View file @
6c2b7b7a
...
...
@@ -124,7 +124,7 @@ Conda environment ${red}snakemake-base_v.${snakemake_base_version}${nc} will be
#
${
red
}
Rename
${
nc
}
: Rename fastq files (ver. 1.601)
#
${
red
}
Graphviz
${
nc
}
: Dot snakemake DAG (ver. 7.1.0)
"
conda
env
create
-f
${
workdir
}
/workflow/environments/
${
os
}
/snakemake-base_v.
${
snakemake_base_version
}
.yaml
q
conda
env
create
-f
${
workdir
}
/workflow/environments/
${
os
}
/snakemake-base_v.
${
snakemake_base_version
}
.yaml
fi
# Remove old 'gevarli' and 'snakemake' environments
...
...
@@ -437,7 +437,7 @@ for directory in ${workdir}/results/02_Mapping/*/ ; do
awk
"NR==1 || NR%2==0"
${
workdir
}
/results/All_
${
reference
}
_genome_coverages.tsv
\
2> /dev/null
\
1>
${
workdir
}
/results/GENCOV.tmp
\
&&
mv
${
workdir
}
/results/GENCOV.tmp
${
workdir
}
/results/All_genome_coverages.tsv
\
&&
mv
${
workdir
}
/results/GENCOV.tmp
${
workdir
}
/results/All_
${
reference
}
_
genome_coverages.tsv
\
2> /dev/null
;
# Concatenate PANGOLIN
cat
${
workdir
}
/results/06_Lineages/
${
reference
}
/
*
_pangolin-report.csv
\
...
...
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configuration/config.yaml
+
3
−
3
View file @
6c2b7b7a
...
...
@@ -30,8 +30,8 @@ consensus:
reference
:
# Your reference, in fasta format (default: SARS-CoV-2_Wuhan_MN-908947-3)
# Available options (not exhaustive), choose one:
-
'
SARS-CoV-2_Wuhan_MN-908947-3'
# SARS-CoV-2 (Nextclade and Pangolin)
#- 'Monkeypox-virus_Zaire_AF-380138-1' # Monkeypox (Nextclade)
#- 'Monkeypox-virus_UK_MT-903345-1' # Monkeypox (Nextclade)
#- 'Monkeypox-virus_Zaire_AF-380138-1' # Monkeypox (Nextclade
and Pangolin
)
#- 'Monkeypox-virus_UK_MT-903345-1' # Monkeypox (Nextclade
and Pangolin
)
#- 'Swinepox-virus_India_MW-036632-1' # Swinepox (Nextclade)
#- 'Ebola-virus_Zaire_AF-272001-1' # Ebola (na)
#- 'Ebola-virus_Sudan_MH-121162-1' # Ebola (Nextclade)
...
...
@@ -142,7 +142,7 @@ conda:
frontend
:
# Conda frontend (default: mamba)
# Available options, choose one:
-
'
mamba'
# mamba (faster)
#- 'conda' # conda
#- 'conda' # conda
(iTrop)
osx
:
# Conda OSX environement yaml files:
snakemake_base
:
'
../environments/osx/snakemake-base_v.2023.04.yaml'
# Snakemake-Base ver. 2023.04
gevarli_tools
:
'
../environments/osx/gevarli-tools_v.2023.04.yaml'
# GeVarLi-Tools ver. 2023.04
...
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