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derip2-0.0.3


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توضیحات

Predict ancestral sequence of fungal repeat elements by correcting for RIP-like mutations in multi-sequence DNA alignments.
ویژگی مقدار
سیستم عامل -
نام فایل derip2-0.0.3
نام derip2
نسخه کتابخانه 0.0.3
نگهدارنده []
ایمیل نگهدارنده []
نویسنده Adam Taranto
ایمیل نویسنده adam.taranto@anu.edu.au
آدرس صفحه اصلی https://github.com/Adamtaranto/deRIP2
آدرس اینترنتی https://pypi.org/project/derip2/
مجوز MIT
[![License: MIT](https://img.shields.io/badge/License-MIT-yellow.svg)](https://opensource.org/licenses/MIT) # deRIP2 Predict progenitor sequence of fungal repeat families by correcting for RIP-like mutations (CpA --> TpA) and cytosine deamination (C --> T) events. Mask RIP or deamination events from input alignment as ambiguous bases. # Table of contents * [Algorithm overview](#algorithm-overview) * [Options and usage](#options-and-usage) * [Installation](#installation) * [Example usage](#example-usage) * [Standard options](#standard-options) * [Issues](#issues) * [License](#license) ## Algorithm overview For each column in input alignment: - Check if number of gapped rows is greater than max gap proportion. If true, then a gap is added to the output sequence. - Set invariant column values in output sequence. - If at least X proportion of bases are C/T or G/A (i.e. maxSNPnoise = 0.4, then at least 0.6 of positions in column must be C/T or G/A). - If reaminate option is set then revert T-->C or A-->G. - If reaminate is not set then check for number of positions in RIP dinucleotide context (C/TpA or TpG/A). - If proportion of positions in column in RIP-like context => minRIPlike threshold, AND at least one substrate and one product motif (i.e. CpA and TpA) is present, perform RIP correction in output sequence. - For all remaining positions in output sequence (not filled by gap, reaminate, or RIP-correction) inherit sequence from input sequence with the fewest observed RIP events (or greatest GC content if not RIP detected or multiple sequences sharing min-RIP count). Outputs: - Corrected sequence as fasta. - Optional, alignment with: - Corrected sequence appended. - Corrected positions masked as ambiguous bases. ## Options and Usage ### Installation Requires Python => v3.6 Clone from this repository: ```bash % git clone https://github.com/Adamtaranto/deRIP2.git && cd deRIP2 && pip install -e . ``` Install from PyPi. ```bash % pip install derip2 ``` Test installation. ```bash # Print version number and exit. % derip2 --version derip2 0.0.3 # Get usage information % derip2 --help ``` ### Example usage For aligned sequences in 'myalignment.fa': - Any column >= 70% gap positions is not corrected. - Bases in column must be >= 80% C/T or G/A - At least 50% bases must be in RIP dinucleotide context (C/T as CpA / TpA) - Inherit all remaining uncorrected positions from least RIP'd sequence. - Mask all substrate and product motifs from corrected columns as ambiguous bases (i.e. CpA to TpA --> YpA) ```bash derip2 --inAln myalignment.fa --format fasta \ --maxGaps 0.7 \ --maxSNPnoise 0.2 \ --minRIPlike 0.5 \ --outDir results \ --outAlnName aligment_with_deRIP.fa \ --label deRIPseqName \ --mask > results/deRIPed_sequence.fa ``` **Output:** - results/deRIPed_sequence.fa - results/masked_aligment_with_deRIP.fa ### Standard options ``` Usage: derip2 [-h] [--version] -i INALN [--format {clustal,emboss,fasta,fasta-m10,ig,nexus,phylip,phylip-sequential,phylip-relaxed,stockholm}] [-g MAXGAPS] [-a] [--maxSNPnoise MAXSNPNOISE] [--minRIPlike MINRIPLIKE] [--fillmaxgc] [--fillindex FILLINDEX] [--mask] [--noappend] [-d OUTDIR] [--outAlnName OUTALNNAME] [--outAlnFormat {fasta,nexus}] [--label LABEL] Predict ancestral sequence of fungal repeat elements by correcting for RIP- like mutations or cytosine deamination in multi-sequence DNA alignments. Optionally, mask corrected positions in alignment. optional arguments: -h, --help show this help message and exit --version show program's version number and exit -i INALN, --inAln INALN Multiple sequence alignment. --format {clustal,emboss,fasta,fasta-m10,ig,nexus,phylip,phylip-sequential,phylip-relaxed,stockholm} Format of input alignment. Default: fasta -g MAXGAPS, --maxGaps MAXGAPS Maximum proportion of gapped positions in column to be tolerated before forcing a gap in final deRIP sequence. Default: 0.7 -a, --reaminate Correct all deamination events independent of RIP context. Default: False --maxSNPnoise MAXSNPNOISE Maximum proportion of conflicting SNPs permitted before excluding column from RIP/deamination assessment. i.e. By default a column with >= 0.5 'C/T' bases will have 'TpA' positions logged as RIP events. Default: 0.5 --minRIPlike MINRIPLIKE Minimum proportion of deamination events in RIP context (5' CpA 3' --> 5' TpA 3') required for column to deRIP'd in final sequence. Note: If 'reaminate' option is set all deamination events will be corrected. Default 0.1 --fillmaxgc By default uncorrected positions in the output sequence are filled from the sequence with the lowest RIP count. If this option is set remaining positions are filled from the sequence with the highest G/C content. Default: False --fillindex FILLINDEX Force selection of alignment row to fill uncorrected positions from by row index number (indexed from 0). Note: Will override '--fillmaxgc' option. --mask Mask corrected positions in alignment with degenerate IUPAC codes. --noappend If set, do not append deRIP'd sequence to output alignment. -d OUTDIR, --outDir OUTDIR Directory for deRIP'd sequence files to be written to. --outAlnName OUTALNNAME Optional: If set write alignment including deRIP corrected sequence to this file. --outAlnFormat {fasta,nexus} Optional: Write alignment including deRIP sequence to file of format X. Default: fasta --label LABEL Use label as name for deRIP'd sequence in output files. ``` ## Issues Submit feedback to the [Issue Tracker](https://github.com/Adamtaranto/deRIP2/issues) ## License Software provided under MIT license.


زبان مورد نیاز

مقدار نام
>= 3.6 Python


نحوه نصب


نصب پکیج whl derip2-0.0.3:

    pip install derip2-0.0.3.whl


نصب پکیج tar.gz derip2-0.0.3:

    pip install derip2-0.0.3.tar.gz