Group-walk: a rigorous approach to group-wise false discovery rate analysis by target-decoy competition

作者
Jack Freestone,Temana Short,William Stafford Noble,Uri Keich
出处
期刊:Bioinformatics [Oxford University Press]
卷期号:38 (Supplement_2): ii82-ii88 被引量:11
标识
DOI:10.1093/bioinformatics/btac471
摘要

MOTIVATION: Target-decoy competition (TDC) is a commonly used method for false discovery rate (FDR) control in the analysis of tandem mass spectrometry data. This type of competition-based FDR control has recently gained significant popularity in other fields after Barber and Candès laid its theoretical foundation in a more general setting that included the feature selection problem. In both cases, the competition is based on a head-to-head comparison between an (observed) target score and a corresponding decoy (knockoff) score. However, the effectiveness of TDC depends on whether the data are homogeneous, which is often not the case: in many settings, the data consist of groups with different score profiles or different proportions of true nulls. In such cases, applying TDC while ignoring the group structure often yields imbalanced lists of discoveries, where some groups might include relatively many false discoveries and other groups include relatively very few. On the other hand, as we show, the alternative approach of applying TDC separately to each group does not rigorously control the FDR. RESULTS: We developed Group-walk, a procedure that controls the FDR in the target-decoy/knockoff setting while taking into account a given group structure. Group-walk is derived from the recently developed AdaPT-a general framework for controlling the FDR with side-information. We show using simulated and real datasets that when the data naturally divide into groups with different characteristics Group-walk can deliver consistent power gains that in some cases are substantial. These groupings include the precursor charge state (4% more discovered peptides at 1% FDR threshold), the peptide length (3.6% increase) and the mass difference due to modifications (26% increase). AVAILABILITY AND IMPLEMENTATION: Group-walk is available at https://cran.r-project.org/web/packages/groupwalk/index.html. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
只是个赠品完成签到,获得积分10
2秒前
赘婿应助王宝宝采纳,获得10
3秒前
四福祥完成签到,获得积分10
4秒前
枫叶完成签到,获得积分10
4秒前
123完成签到,获得积分10
4秒前
4秒前
HJszzZ完成签到,获得积分10
5秒前
5秒前
ken完成签到,获得积分10
6秒前
yuan完成签到 ,获得积分10
6秒前
7秒前
chen完成签到,获得积分10
7秒前
7秒前
zzzy完成签到 ,获得积分10
7秒前
独特的酬海完成签到 ,获得积分20
9秒前
pan发布了新的文献求助10
9秒前
9秒前
时光不染发布了新的文献求助10
10秒前
简单傲柏完成签到,获得积分10
10秒前
雨辰完成签到 ,获得积分10
10秒前
CipherSage应助123321采纳,获得10
11秒前
Present完成签到,获得积分10
11秒前
科研波比发布了新的文献求助10
11秒前
星辰完成签到 ,获得积分10
12秒前
小鱼儿完成签到,获得积分10
12秒前
VDoo完成签到,获得积分10
12秒前
陈思完成签到,获得积分10
12秒前
lili应助饼饼采纳,获得10
13秒前
shaft完成签到,获得积分10
14秒前
kumarr完成签到,获得积分10
15秒前
学术搭子完成签到,获得积分10
15秒前
oymh完成签到 ,获得积分10
15秒前
海天完成签到,获得积分10
16秒前
17秒前
17秒前
隐形青丝完成签到,获得积分10
18秒前
18秒前
小猫咪完成签到,获得积分10
18秒前
dde应助ying采纳,获得10
19秒前
陈陈完成签到,获得积分10
20秒前
高分求助中
Markov Chain Monte Carlo 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Common Foundations of American and East Asian Modernisation: From Alexander Hamilton to Junichero Koizumi 5000
Matrix Methods in Data Mining and Pattern Recognition Second Edition 610
政治传播过程中的外交与说服——以中苏友好协会为例的历史考察 566
Discerning Saints: Moralization of Intrinsic Motivation and Selective Prosociality at Work 500
Handbuch Trainingswissenschaft – Trainingslehre 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7579618
求助须知:如何正确求助?哪些是违规求助? 9159128
关于积分的说明 19593611
捐赠科研通 7162215
什么是DOI,文献DOI怎么找? 3265729
关于科研通互助平台的介绍 2430751
邀请新用户注册赠送积分活动 2256521