daler

"""
https://www.biostars.org/p/152517/

Example of how to work with Ensembl release 81 GTF files, which:

    1) already have genes and transcripts included

    2) have unique IDs for genes, transcripts, and exons in the corresponding
       "<featuretype>_id" attribute

daler

#!/usr/bin/env bash

# Ryan Dale, July 2015
# dalerr@niddk.nih.gov
#
# CollectRnaSeqMetrics.jar from Picard [1] needs an interval list corresponding
# to ribosomal RNA. The format is described at [2].
#
# SAM header creation idea from [3]; idea for using rmsk tables to get rRNA is
# from [4].

daler

The MIT License (MIT)

Copyright (c) 2016 Ryan Dale

Permission is hereby granted, free of charge, to any person obtaining a copy
of this software and associated documentation files (the "Software"), to deal
in the Software without restriction, including without limitation the rights
to use, copy, modify, merge, publish, distribute, sublicense, and/or sell
copies of the Software, and to permit persons to whom the Software is
furnished to do so, subject to the following conditions:

daler

from gffutils.iterators import DataIterator

input_filename = 'example.gff'
output_filename = 'output.gff'

with open(output_filename, 'w') as fout:
    for feature in DataIterator(input_filename):
        # len() works to get the length of a feature in bp
        if len(feature) < 1000:
            continue

daler

#!/bin/bash
set -e
set -o pipefail

# All-in-one installation script to download, configure, and run cloudbiolinux
# to install bioinformatics tools locally without needing sudo. The executables
# will go into $INSTALL_DIR:
INSTALL_DIR=~/tmp/cbl_demo

# See https://github.com/chapmanb/cloudbiolinux for more info on customizing

daler

import pybedtools

# This demo uses files that ship with pybedtools
a = pybedtools.example_bedtool('a.bed')
fasta = pybedtools.example_filename('test.fa')

# Use a properly-formatted BED file, and then post-process the resulting fasta.
x = a.sequence(fi=fasta, s=True)
for i, line in enumerate(open(x.seqfn)):
    if line.startswith('>') and i >0:

daler

##gff-version 3
scaffold_28	prediction	gene	1	402	0	+	.	ID=545184;Name=545184
scaffold_28	prediction	gene	805	981	0	-	.	ID=93782;Name=93782
scaffold_28	prediction	gene	2030	2721	0	+	.	ID=545205;Name=545205
scaffold_28	prediction	gene	3273	3545	0	-	.	Name=YOL159C-A;Synteny=no_synteny;SystematicGeneName=YOL159C-A;ID=38792
scaffold_28	prediction	gene	5318	5833	0	-	.	Name=YOL159C;Synteny=no_synteny;SystematicGeneName=YOL159C;ID=38793
scaffold_28	prediction	gene	6780	8600	0	-	.	Name=ENB1;Synteny=no_synteny;SystematicGeneName=YOL158C;StandardGeneName=ENB1;ID=38794
scaffold_28	prediction	gene	9698	11467	0	-	.	Name=IMA4;Synteny=no_synteny;SystematicGeneName=YJL221C;StandardGeneName=IMA4;ID=38795

daler

This gist provides example data for the metaseq_demo.py script

daler

import pybedtools
import pandas


def split_coverage(x):
    """
    Split a coverage file created using bedtools coverage -hist -- which will
    have trailing "all" hist lines -- into 1) a BedTool object with valid BED
    lines and 2) a pandas DataFrame of all coverage, parsed from the trailing
    "all" lines.

daler

#!/usr/bin/env python

import os
import sys
import platform
import argparse
import ftplib
import time
import netrc
from fnmatch import fnmatch