scDblFinder VS salmon

Compare scDblFinder vs salmon and see what are their differences.

scDblFinder

Methods for detecting doublets in single-cell sequencing data (by plger)
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scDblFinder salmon
1 1
139 742
- 1.9%
6.0 4.1
14 days ago 12 days ago
R C++
GNU General Public License v3.0 only GNU General Public License v3.0 only
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scDblFinder

Posts with mentions or reviews of scDblFinder. We have used some of these posts to build our list of alternatives and similar projects.
  • Are there any methods for doublet deconvolution?
    1 project | /r/bioinformatics | 10 May 2022
    The scDblFinder method identifies doublets by combining singlet profiles to generate artificial doublets, then finding the nearest neighbors to those artificial profiles. You could use this approach to deconvolve your doublets, inferring that the two cells in the actual observed doublet are of the same cell types as those used to generate the nearest artificial doublet profile.

salmon

Posts with mentions or reviews of salmon. We have used some of these posts to build our list of alternatives and similar projects. The last one was on 2023-02-24.
  • Why should academic researchers use Rust?
    3 projects | /r/rust | 24 Feb 2023
    Rust makes distribution and maintenance near trivial. My lab develops a fairly widely-used tool, salmon, for the quantification of transcript expression from RNA-seq data. This tool is written in C++14, and has a substantial number of dependencies. The process of updating the tool (e.g. bumping dependencies) and cutting a new release is painful. To maintain widespread availability, we distribute this tool using bioconda which uses it's own CI and setup to build new releases for (in our case) Linux and MacOS. Things break all the time. For example, recently, they bumped the compiler used to build packages. This changed some default "implementation defined" behavior, causing previously functioning code to fail. We didn't find this locally, because we didn't test that specific compiler version. When we tried to release a new version, we had to go back and fix things etc. This is not just because different compilers exist, but because the C++ specification is soooo complicated and the set of undefined and implementation defined behavior is sooo broad that it's very brittle and it's easy for things to "break" via bitrot. However, the stability provided by Rust has been phenomenal so far. In our code, we only use stable Rust features, and we have benefited tremendously from the empirical guarantee that valid Rust code (except in exceptional cases like latent bugs in the language) will remain valid. While not all crates follow it religiously, there is a reasonable respect for semantic versioning. Thus, cutting a new release of one of our Rust tools is often as simple as just updating the Cargo.toml (and Cargo.lock in the case of applications), tagging a new release in GitHub, and letting the bioconda CI do it's business with the tagged artifacts. The build "scripts" are almost always trivial because the builds just work, across platforms, across CIs, etc. Now, new projects like cargo dist look like they make this process even simpler.

What are some alternatives?

When comparing scDblFinder and salmon you can also consider the following projects:

awesome-single-cell - Community-curated list of software packages and data resources for single-cell, including RNA-seq, ATAC-seq, etc.

rnaseq - RNA-seq analyses.

rnaseqc - Fast, efficient RNA-Seq metrics for quality control and process optimization

noson-app - The essential to control music from your SONOS devices on Linux platforms

gEAR - The gEAR Portal was created as a data archive and viewer for gene expression data including microarrays, bulk RNA-Seq, single-cell RNA-Seq and more.

IntaRNA - Efficient target prediction incorporating accessibility of interaction sites

nanopolish - Signal-level algorithms for MinION data

mixcr - MiXCR is an ultimate software platform for analysis of Next-Generation Sequencing (NGS) data for immune profiling.

mirdeep2 - Discovering known and novel miRNAs from small RNA sequencing data

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