pMoSS (p-value Model using the Sample Size) is a Python code to model the p-value as an n-dependent function using Monte Carlo cross-validation. Exploits the dependence on the sample size to characterize the differences among groups of large datasets
☆16Mar 12, 2024Updated last year
Alternatives and similar repositories for pMoSS
Users that are interested in pMoSS are comparing it to the libraries listed below
Sorting:
- ☆13Apr 27, 2020Updated 5 years ago
- Shell bootloader for data science.☆12Feb 25, 2026Updated last week
- Deep Learning segmentation suite designed for 2D microscopy image segmentation☆10Dec 17, 2021Updated 4 years ago
- analysis tools for large-scale neural recordings☆16Apr 4, 2025Updated 11 months ago
- Source code for the BUDE Alanine Scan web application.☆12May 27, 2025Updated 9 months ago
- List of openly available dataset generated by our lab☆13Jan 9, 2026Updated last month
- Dockerised and simplified version of SeqWare-CGP-SomaticCore☆14Mar 5, 2021Updated 5 years ago
- RAnking Markers for CEll Segmentation☆12Feb 22, 2022Updated 4 years ago
- Single-Cell Sequencing Quality Control and Processing Software☆16Mar 26, 2022Updated 3 years ago
- This is the BWA workflow used in the PanCancer project used to allign all the BAM files.☆11Dec 27, 2022Updated 3 years ago
- ☆12Oct 21, 2018Updated 7 years ago
- some useful function to get Label from ROIs and vice versa , and more!☆11May 3, 2023Updated 2 years ago
- ☆19Apr 6, 2022Updated 3 years ago
- How to use Aligning Big Brains and Atlases with Python☆14May 3, 2023Updated 2 years ago
- Python module to analyse CRISPR-based libraries☆13Apr 1, 2021Updated 4 years ago
- Wormbase Build Pipeline☆22Jan 7, 2026Updated last month
- ilastik plugin for napari☆14Dec 15, 2025Updated 2 months ago
- Code for EpiMap data browser☆14Jun 4, 2024Updated last year
- ☆16Jun 11, 2017Updated 8 years ago
- A napari plugin for stitching large multi-positioning datasets in 2/3D+t using multiview-stitcher☆17Jul 7, 2025Updated 7 months ago
- Improved Ribo-seq enables identification of cryptic translation events☆17Feb 13, 2018Updated 8 years ago
- ☆18May 12, 2023Updated 2 years ago
- Course website for Genomic Data Visualization 2022☆16Dec 28, 2022Updated 3 years ago
- A script that computationally designs a vaccine☆18Jan 9, 2022Updated 4 years ago
- Pipeline for Ribosome Profiling Data☆19Jul 5, 2023Updated 2 years ago
- Standalone cellfinder cell detection algorithm☆20Jan 3, 2024Updated 2 years ago
- python tools for BigDataViewer☆22Dec 29, 2024Updated last year
- ☆19Jun 8, 2023Updated 2 years ago
- k-mer similarity analysis pipeline☆21Nov 20, 2025Updated 3 months ago
- Archived: control, reconstruction, and analysis code for oblique plane microscopy.☆22Apr 1, 2025Updated 11 months ago
- ☆11Jul 3, 2022Updated 3 years ago
- ProSolo, variant calling from single cell DNA-seq data, or: bulk backing vocals for single cell solos.☆21Sep 1, 2021Updated 4 years ago
- BANDITS: Bayesian ANalysis of DIfferenTial Splicing☆19Sep 29, 2025Updated 5 months ago
- Bulk RNA-seq Data Processing, Quality Control, and Downstream Analysis Pipeline☆21Jan 30, 2026Updated last month
- Pathway-based trajectory inference method for time-series scRNAseq data☆25May 18, 2021Updated 4 years ago
- Interface to various variant calling formats.☆31Jun 15, 2024Updated last year
- Combine reference and assembled transcriptomes for RNA-Seq analysis☆24Feb 12, 2020Updated 6 years ago
- Accompanying analysis code for the FRASER manuscript☆25Aug 27, 2020Updated 5 years ago
- Image registration (alignment) software for large microscopy images☆27Oct 15, 2023Updated 2 years ago