Miller lab's modENCODE tiling-array experiments to find Transcriptionally Active Regions. These experiments are designed to detect all C. elegans transcripts by hybridizing RNA to commerically available genome tiling arrays. To maximize the chances of detecting rare transcripts with limited expression in specific cells, RNA was extracted from selected embryonic cells isolated by FACS and from postembryonic cells by use of the mRNA tagging method.
Miller lab's modENCODE tiling-array experiments to find Transcriptionally Active Regions. These experiments are designed to detect all C. elegans transcripts by hybridizing RNA to commerically available genome tiling arrays. To maximize the chances of detecting rare transcripts with limited expression in specific cells, RNA was extracted from selected embryonic cells isolated by FACS and from postembryonic cells by use of the mRNA tagging method.
Miller lab's modENCODE tiling-array experiments to find Transcriptionally Active Regions. These experiments are designed to detect all C. elegans transcripts by hybridizing RNA to commerically available genome tiling arrays. To maximize the chances of detecting rare transcripts with limited expression in specific cells, RNA was extracted from selected embryonic cells isolated by FACS and from postembryonic cells by use of the mRNA tagging method.
Miller lab's modENCODE tiling-array experiments to find Transcriptionally Active Regions. These experiments are designed to detect all C. elegans transcripts by hybridizing RNA to commerically available genome tiling arrays. To maximize the chances of detecting rare transcripts with limited expression in specific cells, RNA was extracted from selected embryonic cells isolated by FACS and from postembryonic cells by use of the mRNA tagging method.
Miller lab's modENCODE tiling-array experiments to find Transcriptionally Active Regions. These experiments are designed to detect all C. elegans transcripts by hybridizing RNA to commerically available genome tiling arrays. To maximize the chances of detecting rare transcripts with limited expression in specific cells, RNA was extracted from selected embryonic cells isolated by FACS and from postembryonic cells by use of the mRNA tagging method.
Miller lab's modENCODE tiling-array experiments to find Transcriptionally Active Regions. These experiments are designed to detect all C. elegans transcripts by hybridizing RNA to commerically available genome tiling arrays. To maximize the chances of detecting rare transcripts with limited expression in specific cells, RNA was extracted from selected embryonic cells isolated by FACS and from postembryonic cells by use of the mRNA tagging method.
Miller lab's modENCODE tiling-array experiments to find Transcriptionally Active Regions. These experiments are designed to detect all C. elegans transcripts by hybridizing RNA to commerically available genome tiling arrays. To maximize the chances of detecting rare transcripts with limited expression in specific cells, RNA was extracted from selected embryonic cells isolated by FACS and from postembryonic cells by use of the mRNA tagging method.
Miller lab's modENCODE tiling-array experiments to find Transcriptionally Active Regions. Peak-calling was done using mSTAD. These experiments are designed to detect all C. elegans transcripts by hybridizing RNA to commerically available genome tiling arrays. To maximize the chances of detecting rare transcripts with limited expression in specific cells, RNA was extracted from selected embryonic cells isolated by FACS and from postembryonic cells by use of the mRNA tagging method.
Miller lab's modENCODE tiling-array experiments to find Transcriptionally Active Regions. Peak-calling was done using mSTAD. These experiments are designed to detect all C. elegans transcripts by hybridizing RNA to commerically available genome tiling arrays. To maximize the chances of detecting rare transcripts with limited expression in specific cells, RNA was extracted from selected embryonic cells isolated by FACS and from postembryonic cells by use of the mRNA tagging method.