Roy, Debasmita J. Kahler, David Yun, Chi Jane Albert Hubbard, E. Supplemental Material for Roy et al., 2018 p.p1 {margin: 0.0px 0.0px 0.0px 0.0px; font: 14.0px Helvetica} <p>Figure S1. Progenitor counts relevant to Figures 1 and 2. (A, B, C)</p><p></p><p>Figure S2. Protocol for “primary” RNAi screen</p><p>Figure S3. Two-step primary RNAi screen selection criteria</p><p></p><p></p><p></p><p></p><p>Figure S4. Separation of <i>rpl-24.2</i> versus C03D6.1 RNAi</p><p>Table S1: Information concerning strains generated or used for this study</p><p>Table S2. Primary screen results</p><p>Table S3. List of 133 genes for which RNAi depletion caused reproducible and elevated penetrance of sterility in glp-1(rf)<br></p><p>Table S4. List of 77 genes for which RNAi depletion caused reproducible and elevated penetrance of sterility in both glp-1(rf) and glp-1(+)<br></p><p>Table S5. PANTHER ‘Statistical Overrepresentation’ analysis of sets of 133 and 56 genes from the Primary screen<br></p><p>Table S6. Summary of n and p values<br></p> p.p1 {margin: 0.0px 0.0px 0.0px 0.0px; font: 10.0px Helvetica} p.p1 {margin: 0.0px 0.0px 0.0px 0.0px; font: 11.0px Helvetica} p.p1 {margin: 0.0px 0.0px 0.0px 0.0px; font: 11.0px Helvetica} TOR;Cyclin-E;MAPK;translation;Cactin;RNA Exosome;Hedgehog-related;Genetics;Developmental Biology;Stem Cells 2018-09-05
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10.25387/g3.6869828.v2