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https://www.dropbox.com/scl/fi/eg9rki2bld2u24bdjy542/PROTEIN-STRUCURES.pptx?rlkey=exrmkb6pfakunhsfqnokjawpm&dl=0 |
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#!/bin/bash | |
# save this file somewhere on your disk. open your terminal, and go there. then type these commands: | |
# | |
# chmod +x anvi-ubuntu-setup.sh | |
# ./anvi-ubuntu-setup.sh | |
# | |
# and then get some coffee, and come back to see whether it's your lucky day. | |
set -e |
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#!/usr/bin/env python | |
# lousy script that works with the outputs of `anvi-export-collection` | |
# to reconcstruct the fate of contigs for a given algorithm and bin and | |
# spit out some text to be visualized on https://app.rawgraphs.io/ | |
import sys | |
from collections import OrderedDict |
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################################################################################# | |
# | |
# PREPARING RELEASE NOTES FOR A MAJOR RELEASE | |
# | |
################################################################################# | |
# if this is a major release, | |
# prepare a new logo. | |
# prepare comprehensive release notes. see examples for release notes here: | |
# https://github.com/meren/anvio/releases |
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#!/bin/bash | |
# A simple loop to serially map all samples. | |
# referenced from within http://merenlab.org/tutorials/assembly_and_mapping/ | |
# how many threads should each mapping task use? | |
NUM_THREADS=4 | |
for sample in `awk '{print $1}' samples.txt` | |
do |
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from anvio.dbops import ContigsSuperclass | |
# if your args object contains a `contigs_db` entry in its | |
# namespace all you don't need the following two lines and | |
# you can directly pass it to the ContigsSuperclass. | |
import argparse | |
args = argparse.Namespace(contigs_db="INFANT-GUT-TUTORIAL/SPLITAH/E_facealis/CONTIGS.db") | |
# get an instance of the contigs super: | |
contigs_db = ContigsSuperclass(args) |
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#!/usr/bin/env python | |
## Antti Karkman | |
## University of Gothenburg | |
## antti.karkman@gmail.com | |
## 2017 | |
import gffutils | |
import argparse |
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# run this script like this: | |
# | |
# python gen_primer_match_report.py primers.txt sequences.txt | |
# | |
# it will generate a report file called `primer_matches_report.txt` | |
# | |
# example primers file (TAB-delimited, no spaces): | |
# | |
# name pair direction sequence | |
# PolF P1 F TGCGAYCCSAARGCBGACTC |
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import sys | |
import IlluminaUtils.lib.fastqlib as u | |
import IlluminaUtils.lib.fastalib as f | |
from IlluminaUtils.utils.helperfunctions import reverse_complement | |
# call this script like this: | |
# | |
# python demultiplex.py barcode_to_sample_name_file index_fastq_file quality_filtered_fasta_file | |
# | |
# expected file formats are shown below. |
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#!/usr/bin/env python | |
# you run this first: | |
# | |
# python 01-gen-nucmer-jobs.py affiliations.txt MAGs_input_dir | |
# | |
import os | |
import sys | |
import anvio.fastalib as u |
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