Last year, Taylor Stanberry caught 60 Burmese pythons with her bares hands—a state record. But this self-taught hunter says ...

Understanding the transformation from a raw chromatogram to a clean sequence is key to accurate bioinformatics analysis. Here’s a breakdown of the formats and the ...

We are living in an era where biology has become synonymous with big data due to the ever-increasing amount of data being generated by technologies such as next-generation sequencing. Bioinformatics ...

Nucleus is a library of Python and C++ code designed to make it easy to read, write and analyze data in common genomics file formats like SAM and VCF. In addition, Nucleus enables painless integration ...

Have you ever wondered how scientists decode the mysteries of life by reading DNA scripts, modeling protein structures, or comparing genetic codes? What if I told you that much of this cutting-edge ...

Our GenBank to FASTA Converter is a seamless web-based utility designed for molecular biologists and bioinformaticians. It efficiently transforms annotated GenBank files into the simplified FASTA ...

Applied Bioinformatics, Department of Computer Science, University of Tübingen, Tübingen 72074, Germany Institute for Bioinformatics and Medical Informatics, University of Tübingen, Tübingen 72074, ...

We present the BioNumPy package, which enables efficient and intuitive array programming on biological data in Python. Internally, this is handled by a ragged data structure (similar to that in ref. 4 ...

The term ‘RNA-seq’ refers to a collection of assays based on sequencing experiments that involve quantifying RNA species from bulk tissue, single cells or single nuclei. The kallisto, bustools and ...

The reconstruction of complete microbial metabolic pathways using ‘omics data from environmental samples remains challenging. Computational pipelines for pathway reconstruction that utilize machine ...