Change Log¶
The record of all notable changes to this project will be documented in this file.
v0.2¶
1 Oct 2020, first release.
v0.9.2¶
12 May 2021, build workflow and create documentation
v0.9.3¶
18 May 2021, bug fix, deal with more tumor types
v0.9.4¶
11 Jun 2021, bug fix, update Scanpy to v1.7.2, deal with the correlation between predicted cell fractions of each cell type and mean gene expression of corresponding marker genes
v0.9.5¶
2 Jul 2021, typo fix, update Scanpy to v1.8.0 & update seaborn to v0.11.1
v0.9.6¶
7 Jul 2021, typo fix, check if Cancer Cells existed and update bbknn to v1.5.1
v0.9.6.1¶
16 Jul 2021, set total_cell_number to 100 and n_base to 3 when simulating bulk cell data for better keeping cell type diversity
v0.9.7¶
13 Sep 2021
Filtering single cell data of CD4 T and CD8 T cells by the ratio of marker genes
Updating marker gene list and re-annotating sub-clustering based on dot-plot figure of each single cell dataset
v0.9.8¶
19 Nov 2021
Building the whole workflow in one file
Recording main parameters and running logs
v1.0.2 (bioRxiv)¶
2 Jun 2023
Update documentation
v1.1.0¶
1 Oct 2023
Update the workflow to contain the following parameters:
alpha_total_rna_coefficient: the coefficient of total RNA for each cell type during the simulation of bulk RNA-seq datacell_type2subtypes: the dictionary of cell types and their subtypes
Update the DNN model to include pathway profiles
Update the documentation
v1.2.0¶
16 Jan 2024
Add GEP-level filtering in the PCA space of TCGA samples
Add Dirichlet distribution to simulate the cellular proportions of bulk RNA-seq data
v1.2.2 (revision)¶
3 Feb 2024
Update the documentation
v1.3.1 (revision)¶
13 Jul 2024
Update Figure 1ab
Update workflow and plot functions during the revision
v1.3.2 (revision)¶
15 Sep 2024
Update documentation