Herald:The Biostar Herald for Tuesday, April 09, 2024
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The Biostar Herald publishes user submitted links of bioinformatics relevance. It aims to provide a summary of interesting and relevant information you may have missed. You too can submit links here.

This edition of the Herald was brought to you by contribution from Istvan Albert, and was edited by Istvan Albert,


submitted by: Istvan Albert


The art of seeing the elephant in the room: 2D embeddings of single-cell data do make sense | bioRxiv (www.biorxiv.org)

More appropriate metrics quantifying neighborhood and class preservation reveal the elephant in the room: while t-SNE and UMAP embeddings of single-cell data do not represent high-dimensional distances, they can nevertheless provide biologically relevant information.

submitted by: Istvan Albert


SeqKit2: A Swiss army knife for sequence and alignment processing (onlinelibrary.wiley.com)

SeqKit2 represents substantial enhancement through the inclusion of 19 additional subcommands, expanding its overall repertoire to a total of 38 in eight categories. The new subcommands add functionality such as amplicon processing and robust, error-tolerant parsing of sequence records. In addition, three subcommands designed for real-time analysis are added for periodic monitoring of properties of FASTQ and Binary Alignment/Map alignment records and real-time streaming from multiple sequence files.

submitted by: Istvan Albert


Snakemake workflows for long-read bacterial genome assembly and evaluation (gigabytejournal.com)

In order to automatically run multiple genome assembly and evaluation programs at once, I developed two workflows for the workflow management system Snakemake, which provide end users with an easy-to-run solution for testing various genome assemblies from their sequencing data. Both workflows use the conda packaging system, so there is no need for manual installation of each program.

submitted by: Istvan Albert


The impact of package selection and versioning on single-cell RNA-seq analysis | bioRxiv (www.biorxiv.org)

We investigate in detail the algorithms and methods underlying Seurat and Scanpy and find that there are, in fact, considerable differences in the outputs of Seurat and Scanpy. The extent of differences between the programs is approximately equivalent to the variability that would be introduced by sequencing less than 5% of the reads for scRNA-seq experiments, or by analyzing less than 20% of the cell population.

submitted by: Istvan Albert


submitted by: Istvan Albert


submitted by: Istvan Albert


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