Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2024 Jan 10;21(2):247–258. doi: 10.1038/s41592-023-02146-w

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

Extended Data Fig. 8 — a, Bar plots showing numbers (left) and percentages (right) of the usable reads and reads filtered in each processing step for ARTR-seq libraries of PTBP1, RBFOX2 and HNRNPC. b, A bar plot showing the usable reads distribution in the intronic (purple), intergenic (grey) and exonic (green) regions for ARTR-seq libraries of PTBP1, RBFOX2 and HNRNPC. c, Cumulative curves and boxplots (inside) showing the absolute value of splicing difference upon RBFOX2 (left) or HNRNPC (right) knockdown. d, Cumulative curves and boxplots (inside) showing the absolute value of splicing differences of included RI upon PTBP1 knockdown. In c,d, RBP-regulated genes were divided into three groups according to their enrichment in ARTR-seq, including no enrichment (No, 0 ≤ enrichment ≤ 1), low enrichment (Low, 1 < enrichment ≤ 2) and high enrichment (High, 2 < enrichment). The sample size in c,d was indicated below the respective box. P-values in c,d were determined using the two-tailed Student’s t-test of indicated group versus ‘no enrichment’ group.