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Number of human protein variations collected from the UniProt/Swiss-Prot database.

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数据链接：

https://figshare.com/articles/dataset/_Number_of_human_protein_variations_collected_from_the_UniProt_Swiss_Prot_database_/233492 数据链接链接失效反馈

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资源简介：

Number of human protein variations collected from the UniProt/Swiss-Prot database.

应用场景：

创建时间：

2012-10-08

蛋白质变异

基因测序

Additional file 8: Table S5. Baseline Kir2.1 library errors. Error counts within the sequencing data. Because Illumina sequencing platforms have baseline error rates to a degree this is a combined err

DataCite Commons2024-08-13 更新130

Additional file 4 of DIMPLE: deep insertion, deletion, and missense mutation libraries for exploring protein variation in evolution, disease, and biology

蛋白质变异

基因分析

Additional file 4: Table S1. Inputs and outputs from test running DIMPLE. As discussed within the text, we tested the computational DIMPLE pipeline by including 25 genes. Within this table is their le

DataCite Commons2024-08-14 更新90

Chr16-HPP. Shotgun Analysis improvement. JPR HPP Special issue 2013. MCF7 Cell line.

人类蛋白质组

MCF7细胞系

The Chromosome 16 Consortium is integrated in the Human Proteome Project that aims to develop an entire map of the proteins encoded by the human genome following a gene-centric strategy (C-HPP) to mak

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MOESM4 of Natural and pathogenic protein sequence variation affecting prion-like domains within and across human proteomes

蛋白质变异

翻译后修饰

Additional file 4. Comprehensive mapping of PTMs within moderately high-scoring human PrLDs. Human PTMs derived from the ActiveDriverDB were mapped to all human PrLDs with PAPA score > 0.0. For eac

DataCite Commons2020-08-26 更新110

Additional file 1 of DIMPLE: deep insertion, deletion, and missense mutation libraries for exploring protein variation in evolution, disease, and biology

蛋白质变异

基因编辑

Additional file 1. Agilent Sure Print OLS Pool. Names and sequences for the OLS pools that we used to build libraries for this study.

DataCite Commons2024-08-14 更新60