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Docs: point to bcbio organization repository
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chapmanb committed Mar 9, 2018
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1 change: 1 addition & 0 deletions .gitignore
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Expand Up @@ -28,3 +28,4 @@ cwl/*-workflow
.idea/
__pycache__
.coverage
.pytest_cache
4 changes: 2 additions & 2 deletions Dockerfile
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Expand Up @@ -12,7 +12,7 @@ RUN apt-get update && \
# bcbio-nextgen installation
mkdir -p /tmp/bcbio-nextgen-install && cd /tmp/bcbio-nextgen-install && \
wget --no-check-certificate \
https://raw.github.com/chapmanb/bcbio-nextgen/master/scripts/bcbio_nextgen_install.py && \
https://raw.github.com/bcbio/bcbio-nextgen/master/scripts/bcbio_nextgen_install.py && \
python bcbio_nextgen_install.py /usr/local/share/bcbio-nextgen \
--isolate --minimize-disk --nodata -u development && \
git config --global url.https://github.com/.insteadOf git://github.com/ && \
Expand All @@ -28,7 +28,7 @@ RUN apt-get update && \

# add user run script
wget --no-check-certificate -O createsetuser \
https://raw.github.com/chapmanb/bcbio-nextgen-vm/master/scripts/createsetuser && \
https://raw.github.com/bcbio/bcbio-nextgen-vm/master/scripts/createsetuser && \
chmod a+x createsetuser && mv createsetuser /sbin && \

# clean filesystem
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12 changes: 6 additions & 6 deletions README.rst
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Expand Up @@ -10,8 +10,8 @@ provides a shared community resource that handles the data processing component
of sequencing analysis, providing researchers with more time to focus on the
downstream biology.

.. image:: https://travis-ci.org/chapmanb/bcbio-nextgen.png
:target: https://travis-ci.org/chapmanb/bcbio-nextgen
.. image:: https://travis-ci.org/bcbio/bcbio-nextgen.png
:target: https://travis-ci.org/bcbio/bcbio-nextgen

Features
--------
Expand Down Expand Up @@ -55,7 +55,7 @@ Quick start

1. `Install`_ ``bcbio-nextgen`` with all tool dependencies and data files::

wget https://raw.github.com/chapmanb/bcbio-nextgen/master/scripts/bcbio_nextgen_install.py
wget https://raw.github.com/bcbio/bcbio-nextgen/master/scripts/bcbio_nextgen_install.py
python bcbio_nextgen_install.py /usr/local/share/bcbio --tooldir=/usr/local \
--genomes GRCh37 --aligners bwa --aligners bowtie2

Expand All @@ -74,8 +74,8 @@ Quick start
cd project1/work
bcbio_nextgen.py ../config/project1.yaml -n 8

.. _system configuration file: https://github.com/chapmanb/bcbio-nextgen/blob/master/config/bcbio_system.yaml
.. _sample description file: https://github.com/chapmanb/bcbio-nextgen/blob/master/config/bcbio_sample.yaml
.. _system configuration file: https://github.com/bcbio/bcbio-nextgen/blob/master/config/bcbio_system.yaml
.. _sample description file: https://github.com/bcbio/bcbio-nextgen/blob/master/config/bcbio_sample.yaml
.. _Automatically create a processing description: https://bcbio-nextgen.readthedocs.org/en/latest/contents/configuration.html#automated-sample-configuration
.. _Install: https://bcbio-nextgen.readthedocs.org/en/latest/contents/installation.html#automated
.. _configuration options: https://bcbio-nextgen.readthedocs.org/en/latest/contents/configuration.html
Expand All @@ -88,7 +88,7 @@ See the `full documentation`_ and `longer analysis-based articles
and discussion on the `biovalidation mailing list`_.

.. _full documentation: https://bcbio-nextgen.readthedocs.org
.. _GitHub: https://github.com/chapmanb/bcbio-nextgen/issues
.. _GitHub: https://github.com/bcbio/bcbio-nextgen/issues
.. _biovalidation mailing list: https://groups.google.com/d/forum/biovalidation

Contributors
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2 changes: 1 addition & 1 deletion bcbio/broad/__init__.py
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Expand Up @@ -26,7 +26,7 @@ def get_default_jvm_opts(tmp_dir=None, parallel_gc=False):
Avoids issues with multiple spun up Java processes running into out of memory errors.
Parallel GC can use a lot of cores on big machines and primarily helps reduce task latency
and responsiveness which are not needed for batch jobs.
https://github.com/chapmanb/bcbio-nextgen/issues/532#issuecomment-50989027
https://github.com/bcbio/bcbio-nextgen/issues/532#issuecomment-50989027
https://wiki.csiro.au/pages/viewpage.action?pageId=545034311
http://stackoverflow.com/questions/9738911/javas-serial-garbage-collector-performing-far-better-than-other-garbage-collect
However, serial GC causes issues with Spark local runs so we use parallel for those cases:
Expand Down
6 changes: 3 additions & 3 deletions bcbio/install.py
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Expand Up @@ -29,10 +29,10 @@
from bcbio.pipeline import datadict as dd

REMOTES = {
"requirements": "https://raw.githubusercontent.com/chapmanb/bcbio-nextgen/master/requirements-conda.txt",
"gitrepo": "https://github.com/chapmanb/bcbio-nextgen.git",
"requirements": "https://raw.githubusercontent.com/bcbio/bcbio-nextgen/master/requirements-conda.txt",
"gitrepo": "https://github.com/bcbio/bcbio-nextgen.git",
"cloudbiolinux": "https://github.com/chapmanb/cloudbiolinux/archive/master.tar.gz",
"genome_resources": "https://raw.github.com/chapmanb/bcbio-nextgen/master/config/genomes/%s-resources.yaml",
"genome_resources": "https://raw.github.com/bcbio/bcbio-nextgen/master/config/genomes/%s-resources.yaml",
"snpeff_dl_url": ("http://downloads.sourceforge.net/project/snpeff/databases/v{snpeff_ver}/"
"snpEff_v{snpeff_ver}_{genome}.zip")}
SUPPORTED_GENOMES = ["GRCh37", "hg19", "hg38", "hg38-noalt", "mm10", "mm9",
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2 changes: 1 addition & 1 deletion bcbio/pipeline/rnaseq.py
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Expand Up @@ -74,7 +74,7 @@ def run_rnaseq_variant_calling(data):
if isinstance(variantcaller, list) and len(variantcaller) > 1:
logger.error("Only one variantcaller can be run for RNA-seq at "
"this time. Post an issue here "
"(https://github.com/chapmanb/bcbio-nextgen/issues) "
"(https://github.com/bcbio/bcbio-nextgen/issues) "
"if this is something you need to do.")
sys.exit(1)

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2 changes: 1 addition & 1 deletion bcbio/rnaseq/kallisto.py
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Expand Up @@ -30,7 +30,7 @@ def run_kallisto_rnaseq(data):
assert file_exists(fasta_file), "%s was not found, exiting." % fasta_file
assert fq2, ("bcbio doesn't support kallisto for single-end reads, we can "
"add support for this if you open up an issue about it here: "
"https://github.com/chapmanb/bcbio-nextgen/issues")
"https://github.com/bcbio/bcbio-nextgen/issues")
out_file = kallisto_rnaseq(fq1, fq2, kallisto_dir, gtf_file, fasta_file, data)
data = dd.set_kallisto_quant(data, out_file)
return [[data]]
Expand Down
2 changes: 1 addition & 1 deletion bcbio/rnaseq/umi.py
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Expand Up @@ -294,7 +294,7 @@ def demultiplex_samples(data):
files = data["files"]
if len(files) == 2:
logger.error("Sample demultiplexing doesn't handle paired-end reads, but "
"we can add it. Open an issue here https://github.com/chapmanb/bcbio-nextgen/issues if you need this and we'll add it.")
"we can add it. Open an issue here https://github.com/bcbio/bcbio-nextgen/issues if you need this and we'll add it.")
sys.exit(1)
else:
fq1 = files[0]
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4 changes: 2 additions & 2 deletions bcbio/structural/cnvkit.py
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Expand Up @@ -297,7 +297,7 @@ def _cnvkit_segment(cnr_file, cov_interval, data, items, out_file=None):
if cov_interval == "genome":
cmd += ["--threshold", "0.00001"]
# For tumors, remove very low normalized regions, avoiding upcaptured noise
# https://github.com/chapmanb/bcbio-nextgen/issues/2171#issuecomment-348333650
# https://github.com/bcbio/bcbio-nextgen/issues/2171#issuecomment-348333650
paired = vcfutils.get_paired(items)
if paired:
cmd += ["--drop-low-coverage"]
Expand Down Expand Up @@ -407,7 +407,7 @@ def _get_batch_gender(items):
Better not to specify for mixed populations, CNVkit will work
it out
https://github.com/chapmanb/bcbio-nextgen/commit/1a0e217c8a4d3cee10fa890fb3cfd4db5034281d#r26279752
https://github.com/bcbio/bcbio-nextgen/commit/1a0e217c8a4d3cee10fa890fb3cfd4db5034281d#r26279752
"""
genders = set([population.get_gender(x) for x in items])
if len(genders) == 1:
Expand Down
4 changes: 2 additions & 2 deletions bcbio/variation/bedutils.py
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Expand Up @@ -23,8 +23,8 @@ def get_sort_cmd(tmp_dir=None):
This also fixes versions of sort, like 8.22 in CentOS 7.1, that have broken
sorting without version sorting specified.
https://github.com/chapmanb/bcbio-nextgen/issues/624
https://github.com/chapmanb/bcbio-nextgen/issues/1017
https://github.com/bcbio/bcbio-nextgen/issues/624
https://github.com/bcbio/bcbio-nextgen/issues/1017
"""
has_versionsort = subprocess.check_output("sort --help | grep version-sort; exit 0", shell=True).strip()
if has_versionsort:
Expand Down
2 changes: 1 addition & 1 deletion bcbio/variation/recalibrate.py
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Expand Up @@ -150,7 +150,7 @@ def _gatk_apply_bqsr(data):
params = ["-T", "PrintReads", "-R", dd.get_ref_file(data), "-I", in_file,
"-BQSR", data["prep_recal"], "-o", tx_out_file]
# Avoid problems with intel deflater for GATK 3.8 and GATK4
# https://github.com/chapmanb/bcbio-nextgen/issues/2145#issuecomment-343095357
# https://github.com/bcbio/bcbio-nextgen/issues/2145#issuecomment-343095357
if gatk_type == "gatk4":
params += ["--jdk-deflater", "--jdk-inflater"]
elif LooseVersion(broad_runner.gatk_major_version()) > LooseVersion("3.7"):
Expand Down
2 changes: 1 addition & 1 deletion bcbio/variation/validate.py
Original file line number Diff line number Diff line change
Expand Up @@ -283,7 +283,7 @@ def _pick_best_quality_score(vrn_file):
Implementation based on discussion:
https://github.com/chapmanb/bcbio-nextgen/commit/a538cecd86c0000d17d3f9d4f8ac9d2da04f9884#commitcomment-14539249
https://github.com/bcbio/bcbio-nextgen/commit/a538cecd86c0000d17d3f9d4f8ac9d2da04f9884#commitcomment-14539249
(RTG=AVR/GATK=VQSLOD/MuTect=t_lod_fstar, otherwise GQ, otherwise QUAL, otherwise DP.)
Expand Down
2 changes: 1 addition & 1 deletion bcbio/workflow/template.py
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Expand Up @@ -150,7 +150,7 @@ def name_to_config(template):
with open(template) as in_handle:
config = yaml.load(in_handle)
else:
base_url = "https://raw.github.com/chapmanb/bcbio-nextgen/master/config/templates/%s.yaml"
base_url = "https://raw.github.com/bcbio/bcbio-nextgen/master/config/templates/%s.yaml"
try:
with contextlib.closing(urllib.request.urlopen(base_url % template)) as in_handle:
txt_config = in_handle.read()
Expand Down
2 changes: 1 addition & 1 deletion config/examples/HCC2218-sv-getdata.sh
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Expand Up @@ -6,7 +6,7 @@ set -eu -o pipefail

mkdir -p config
cd config
wget -c https://raw.githubusercontent.com/chapmanb/bcbio-nextgen/master/config/examples/HCC2218-sv.yaml
wget -c https://raw.githubusercontent.com/bcbio/bcbio-nextgen/master/config/examples/HCC2218-sv.yaml
cd ../

mkdir -p input
Expand Down
2 changes: 1 addition & 1 deletion config/examples/NA12878-exome-methodcmp-getdata.sh
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Expand Up @@ -10,7 +10,7 @@ set -eu -o pipefail

mkdir -p config
cd config
wget https://raw.github.com/chapmanb/bcbio-nextgen/master/config/examples/NA12878-exome-methodcmp.yaml
wget https://raw.github.com/bcbio/bcbio-nextgen/master/config/examples/NA12878-exome-methodcmp.yaml
cd ..

mkdir -p input
Expand Down
2 changes: 1 addition & 1 deletion config/examples/NA12878-hg38-validate-getdata.sh
Original file line number Diff line number Diff line change
Expand Up @@ -7,7 +7,7 @@ set -eu -o pipefail

mkdir -p config
cd config
wget -c https://raw.githubusercontent.com/chapmanb/bcbio-nextgen/master/config/examples/NA12878-hg38-validate.yaml
wget -c https://raw.githubusercontent.com/bcbio/bcbio-nextgen/master/config/examples/NA12878-hg38-validate.yaml
cd ..

mkdir -p input
Expand Down
2 changes: 1 addition & 1 deletion config/examples/NA12878-sv-getdata.sh
Original file line number Diff line number Diff line change
Expand Up @@ -9,7 +9,7 @@ set -eu -o pipefail

mkdir -p config
cd config
wget -c https://raw.githubusercontent.com/chapmanb/bcbio-nextgen/master/config/examples/NA12878-sv.yaml
wget -c https://raw.githubusercontent.com/bcbio/bcbio-nextgen/master/config/examples/NA12878-sv.yaml
cd ..

mkdir -p input
Expand Down
2 changes: 1 addition & 1 deletion config/examples/NA24385-10x-getdata.sh
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Expand Up @@ -29,7 +29,7 @@ cd ..

mkdir -p config
cd config
wget -c https://raw.githubusercontent.com/chapmanb/bcbio-nextgen/master/config/examples/NA24385-10x.yaml
wget -c https://raw.githubusercontent.com/bcbio/bcbio-nextgen/master/config/examples/NA24385-10x.yaml
cd ..

mkdir -p work
2 changes: 1 addition & 1 deletion config/examples/cancer-giab-na12878-na24385-getdata.sh
Original file line number Diff line number Diff line change
Expand Up @@ -7,7 +7,7 @@ set -eu -o pipefail

mkdir -p config
cd config
wget -c https://raw.githubusercontent.com/chapmanb/bcbio-nextgen/master/config/examples/cancer-giab-na12878-na24385.yaml
wget -c https://raw.githubusercontent.com/bcbio/bcbio-nextgen/master/config/examples/cancer-giab-na12878-na24385.yaml
cd ..

base_url=ftp://ftp-trace.ncbi.nlm.nih.gov/giab/ftp/use_cases/mixtures/UMCUTRECHT_NA12878_NA24385_mixture_10052016
Expand Down
2 changes: 1 addition & 1 deletion config/examples/giab-validate-setup.sh
Original file line number Diff line number Diff line change
Expand Up @@ -9,7 +9,7 @@ set -eu -o pipefail

mkdir -p config
cd config
wget -c https://raw.githubusercontent.com/chapmanb/bcbio-nextgen/master/config/examples/giab-validate.yaml
wget -c https://raw.githubusercontent.com/bcbio/bcbio-nextgen/master/config/examples/giab-validate.yaml
cd ..

mkdir -p input
Expand Down
4 changes: 2 additions & 2 deletions config/examples/rnaseq-seqc-getdata.sh
Original file line number Diff line number Diff line change
Expand Up @@ -7,7 +7,7 @@ df --block-size=G --output='avail' . | sed s/G//g | awk -v req_disk_space=${REQ_

mkdir -p seqc-test/input
cd seqc-test
wget --no-check-certificate https://raw.githubusercontent.com/chapmanb/bcbio-nextgen/master/config/examples/rnaseq-seqc.yaml
wget --no-check-certificate https://raw.githubusercontent.com/bcbio/bcbio-nextgen/master/config/examples/rnaseq-seqc.yaml

cd input
for SAMPLE in SRR950078 SRR950079 SRR950080 SRR950081 SRR950082 SRR950083
Expand All @@ -16,7 +16,7 @@ do
wget -O ${SAMPLE}_2.fastq.gz ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR950/${SAMPLE}/${SAMPLE}_2.fastq.gz
done

wget --no-check-certificate https://raw.githubusercontent.com/chapmanb/bcbio-nextgen/master/config/examples/seqc.csv
wget --no-check-certificate https://raw.githubusercontent.com/bcbio/bcbio-nextgen/master/config/examples/seqc.csv

cd ../
bcbio_nextgen.py -w template rnaseq-seqc.yaml input/seqc.csv input
2 changes: 1 addition & 1 deletion config/galaxy/bcbio/variant.xml
Original file line number Diff line number Diff line change
Expand Up @@ -70,6 +70,6 @@ details:
<help>
SNP and indel variant calling using `bcbio-nextgen`_.

.. _bcbio-nextgen: https://github.com/chapmanb/bcbio-nextgen
.. _bcbio-nextgen: https://github.com/bcbio/bcbio-nextgen
</help>
</tool>
2 changes: 1 addition & 1 deletion config/teaching/cancer-syn3-chr6-prep.sh
Original file line number Diff line number Diff line change
Expand Up @@ -11,7 +11,7 @@ rm -f cancer-syn3-chr6-input.tar.gz

mkdir -p config
cd config
wget -c https://raw.githubusercontent.com/chapmanb/bcbio-nextgen/master/config/teaching/cancer-syn3-chr6.yaml
wget -c https://raw.githubusercontent.com/bcbio/bcbio-nextgen/master/config/teaching/cancer-syn3-chr6.yaml
cd ..

mkdir -p work
6 changes: 3 additions & 3 deletions docs/contents/citations.rst
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@@ -1,19 +1,19 @@
Citations
---------

https://github.com/chapmanb/bcbio-nextgen
https://github.com/bcbio/bcbio-nextgen

small RNA-seq
=============

Data was analyzed with bcbio-nextgen (https://github.com/chapmanb/bcbio-nextgen)
Data was analyzed with bcbio-nextgen (https://github.com/bcbio/bcbio-nextgen)
using piDNA to detect the adapter, cutadapt to remove it, STAR/bowtie to align against
the genome and seqcluster to detect small RNA transcripts. miRNAs were detected using
miraligner tool with miRBase as the reference miRNA database. tRNA profiles were
detected using tdrmapper tool. mirdeep2 was used for discovery of novel miRNAs. FastQC
was used for QC metrics and multiqc for reporting.

Download BIB format: https://github.com/chapmanb/bcbio-nextgen/tree/master/docs/contents/misc/bcbio-smallrna.bib
Download BIB format: https://github.com/bcbio/bcbio-nextgen/tree/master/docs/contents/misc/bcbio-smallrna.bib

Tools
~~~~~
Expand Down
6 changes: 3 additions & 3 deletions docs/contents/cloud.rst
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Expand Up @@ -9,7 +9,7 @@ perform analyses at scale with no investment in local hardware. They also offer
full programmatic control over the environment, allowing bcbio to automate the
entire setup, run and teardown process.

`bcbio-vm <https://github.com/chapmanb/bcbio-nextgen-vm>`_ provides a wrapper
`bcbio-vm <https://github.com/bcbio/bcbio-nextgen-vm>`_ provides a wrapper
around bcbio-nextgen that automates interaction with AWS and `Docker
<https://www.docker.com/>`_. ``bcbio_vm.py`` also cleans up the command line
usage to make it more intuitive and provides a superset of functionality
Expand Down Expand Up @@ -284,7 +284,7 @@ And plot, slice, zoom it in an jupyter notebook using matplotlib,
[highcharts](https://github.com/arnoutaertgeerts/python-highcharts).

In addition to plots, the
`summarize_timing.py <https://github.com/chapmanb/bcbio-nextgen/blob/master/scripts/utils/summarize_timing.py>`_
`summarize_timing.py <https://github.com/bcbio/bcbio-nextgen/blob/master/scripts/utils/summarize_timing.py>`_
utility script prepares a summary table of run times per step.

Shutting down
Expand Down Expand Up @@ -312,5 +312,5 @@ that automatically reads and writes these configurations to avoid users needing
to understand elasticluster internals, but all functionality is fully available.
Edit your ``~/.bcbio/elasticluster/config`` file to change parameters. You can
also see the `latest example configuration
<https://github.com/chapmanb/bcbio-nextgen-vm/blob/master/elasticluster/config>`_.
<https://github.com/bcbio/bcbio-nextgen-vm/blob/master/elasticluster/config>`_.
in the bcbio-vm GitHub repository for more details on the other available options.
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