期刊
NATURE METHODS
卷 6, 期 1, 页码 47-54出版社
NATURE RESEARCH
DOI: 10.1038/NMETH.1279
关键词
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资金
- US National Institutes of Health [R01 HG001715, R01 HG003224, F32 HG004098, T32 CA09361]
- University of Ghent [GOA12051401]
- Fonds Wetenschappelijk Onderzoek - Vlaanderen (FWO-V) [G.0031.06]
- US Department of the Army [W81XWH-04-1-0307]
- State of New York's Science and Tech Resources [C040066]
- Fonds de la Recherche Scientifique (FRS-FNRS, French Community of Belgium).
- NATIONAL CANCER INSTITUTE [T32CA009361] Funding Source: NIH RePORTER
- NATIONAL HUMAN GENOME RESEARCH INSTITUTE [R01HG003224, F32HG004098, R01HG001715] Funding Source: NIH RePORTER
To provide accurate biological hypotheses and elucidate global properties of cellular networks, systematic identification of protein-protein interactions must meet high quality standards. We present an expanded C. elegans protein-protein interaction network, or 'interactome' map, derived from testing a matrix of similar to 10,000 x similar to 10,000 proteins using a highly specific, high-throughput yeast two-hybrid system. Through a new empirical quality control framework, we show that the resulting data set ( Worm Interactome 2007, or WI-2007) was similar in quality to low-throughput data curated from the literature. We filtered previous interaction data sets and integrated them with WI-2007 to generate a high-confidence consolidated map ( Worm Interactome version 8, or WI8). This work allowed us to estimate the size of the worm interactome at similar to 116,000 interactions. Comparison with other types of functional genomic data shows the complementarity of distinct experimental approaches in predicting different functional relationships between genes or proteins.
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