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This excerpt taken from the AFFX 10-K filed Jul 30, 2007. National
Cancer Institute. In
January 2001, we entered into a collaboration agreement with the National
Cancer Institute on a human transcriptome initiative which seeks to construct
maps locating the sites of RNA transcription across the entire human genome
using high-density whole-genome arrays interrogating at resolutions and
throughput rates never before attempted. The transcriptome is defined as the
complete collection of transcribed elements of the genome. In addition to
mRNAs, it also represents non-coding RNAs that are used for structural and gene
regulation purposes. Alterations in the structure or levels of expression of
any one of these RNAs or their proteins could contribute to disease. An
understanding of the transcriptome may provide valuable insights in the
research for novel drugs. We have made the data from this initiative freely
available to the public via the Web through a version of the data integration
and analysis software platform developed by Biotique Systems, Inc., a
company that provides decision support tools and services for the emerging
field of pharmacogenomics. We are using the Biotique Local Integration System
to house this transcriptome data and to provide an interface for researchers to
access, query and use this information. This collaboration was extended during
fiscal 2003 to address the identification of transcriptional binding sites,
methylation sites, origins of replication and other genomic features.
This excerpt taken from the AFFX 10-K filed Mar 1, 2007. National
Cancer Institute. In
January 2001, we entered into a collaboration agreement with the National
Cancer Institute on a human transcriptome initiative which seeks to construct
maps locating the sites of RNA transcription across the entire human genome
using high-density whole-genome tiling arrays interrogating at
resolutions and throughput rates never before attempted. The transcriptome is
defined as the complete collection of transcribed elements of the genome. In
addition to well characterized protein coding transcripts, it also represents
non-coding RNAs that are used for structural and gene regulatory purposes.
Alterations in the structure or levels of expression of any one of these RNAs
or their proteins could contribute to disease. An understanding of the
transcriptome may provide valuable insights in the research for novel drugs. We
have made the data from this initiative freely available to the public
databases located at the National Cancer Institute, UC Santa Cruz, GeneExpress,
and Affymetrix public websites. This collaboration was extended during fiscal
2003 through mid 2007 to complete the transcript mapping of the entire human
genome. In addition to studies performed to detect sites of transcription our
technology has been used to map sites of binding by transcription factor
regulatory elements, modication of chromatin proteins and DNA and genomic
origins of DNA replication.
This excerpt taken from the AFFX 10-K filed Aug 30, 2006. National
Cancer Institute. In
January 2001, we entered into a collaboration agreement with the National
Cancer Institute on a human transcriptome initiative which seeks to construct
maps locating the sites of RNA transcription across the entire human genome
using high-density whole-genome arrays interrogating at resolutions and
throughput rates never before attempted. The transcriptome is defined as the
complete collection of transcribed elements of the genome. In addition to
mRNAs, it also represents non-coding RNAs that are used for structural and gene
regulation purposes. Alterations in the structure or levels of expression of
any one of these RNAs or their proteins could contribute to disease. An
understanding of the transcriptome may provide valuable insights in the
research for novel drugs. We have made the data from this initiative freely
available to the public via the Web through a version of the data integration
and analysis software platform developed by Biotique Systems, Inc., a
company that provides decision support tools and services for the emerging
field of pharmacogenomics. We are using the Biotique Local Integration System
to house this transcriptome data and to provide an interface for researchers to
access, query and use this information. This collaboration was extended during
fiscal 2003 to address the identification of transcriptional binding sites,
methylation sites, origins of replication and other genomic features.
This excerpt taken from the AFFX 10-K filed Mar 9, 2006. National
Cancer Institute. In
January 2001, we entered into a collaboration agreement with the National
Cancer Institute on a human transcriptome initiative which seeks to construct
maps locating the sites of RNA transcription across the entire human genome
using high-density whole-genome arrays interrogating at resolutions and
throughput rates never before attempted. The transcriptome is defined as the
complete collection of transcribed elements of the genome. In addition to
mRNAs, it also represents non-coding RNAs that are used for structural and gene
regulation purposes. Alterations in the structure or levels of expression of
any one of these RNAs or their proteins could contribute to disease. An
understanding of the transcriptome may provide valuable insights in the
research for novel drugs. We have made the data from this initiative freely
available to the public via the Web through a version of the data integration
and analysis software platform developed by Biotique Systems, Inc., a
company that provides decision support tools and services for the emerging
field of pharmacogenomics. We are using the Biotique Local Integration System
to house this transcriptome data and to provide an interface for researchers to
access, query and use this information. This collaboration was extended during
fiscal 2003 to address the identification of transcriptional binding sites,
methylation sites, origins of replication and other genomic features.
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