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a C library for reading/writing high-throughput sequencing data.

a high-throughput program for aligning a file of short DNA sequencing reads against a protein reference database such as NR, at 20,000 times the speed of BLASTX, with high sensitivity.

an implementation of the inference pipeline of AlphaFold v2.0 using a completely new model that was entered in CASP14.

a computational tool to analyze TCR and BCR sequences using unselected RNA sequencing data, profiled from fluid and solid tissues, including tumors.

a software platform for working with genomic data such as sequencing reads, sequences, per-base numeric values or annotations written in Java.

a tool designed to build mechanistic models - i.e. models that simulates a biological process.

a free software environment for statistical computing and graphics.

genomic variant annotation and functional effect prediction toolbox.

a general-purpose, interpreted, object oriented, high-level dynamic programming language that emphasizes code readability. Its syntax allows programmers to express concepts in fewer lines of code than in C++ or Java, thus allowing programmers to work more quickly and integrate their systems more effectively.

a free software environment for statistical computing and graphics.