Biopython for Windows (x64 bit) 1.80 freeware
Biopython for Windows x64 is a set of freely available tools for biological computation written in Python by an international team of developers.
It is a distributed collaborative effort to develop Python libraries and applications which address the needs of current and future work in bioinformatics. The source code is made available under the Biopython License, which is extremely liberal and compatible with almost every license ...
| Author | Biopython.org |
| Released | 2022-11-18 |
| Filesize | 2.30 MB |
| Downloads | 1198 |
| OS | Windows Vista x64, Windows 7 x64, Windows 8 x64, Windows 10 x64, Windows 11 |
| Installation | Instal And Uninstall |
| Keywords | x64 python, Windows x64 |
| Users' rating (7 rating) |
Biopython for Windows (x64 bit) Free Download - we do not host any Biopython for Windows (x64 bit) torrent files or links of Biopython for Windows (x64 bit) on rapidshare.com, depositfiles.com, megaupload.com etc. All Biopython for Windows (x64 bit) download links are direct Biopython for Windows (x64 bit) download from publisher site or their selected mirrors.
| 1.80 | Nov 18, 2022 | New Release | |
| 1.79 | Jun 3, 2021 | New Release | |
| 1.66 | Nov 2, 2015 | New Release | Further work on the Bio.KEGG and Bio.Graphics modules now allows drawing KGML pathways with transparency. The Bio.SeqIO "abi" parser now decodes almost all the documented fields used by the ABIF instruments - including the individual color channels. Bio.PDB now has a QCPSuperimposer module using the Quaternion Characteristic Polynomial algorithm for superimposing structures. This is a fast alternative to the existing SVDSuperimposer code using singular value decomposition. Bio.Entrez now implements the NCBI Entrez Citation Matching function (ECitMatch), which retrieves PubMed IDs (PMIDs) that correspond to a set of input citation strings. Bio.Entrez.parse(...) now supports NCBI XML files using XSD schemas, which will be downloaded and cached like NCBI DTD files. A subtle bug in how multi-part GenBank/EMBL locations on the reverse strand were parsed into CompoundLocations was fixed: complement(join(...)) as used by NCBI worked, but join(complement(...),complement(...),...) |
