SRX1044130 GSM1700709 SRP058873 SRS949623 GSM1700709 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700709 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700709 gds 301700709 GEO Accession GSM1700709 SRX1044131 GSM1700710 SRP058873 SRS949622 GSM1700710 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700710 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700710 gds 301700710 GEO Accession GSM1700710 SRX1044132 GSM1700669 SRP058873 SRS949621 GSM1700669 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700669 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700669 gds 301700669 GEO Accession GSM1700669 SRX1044133 GSM1700670 SRP058873 SRS949620 GSM1700670 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700670 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700670 gds 301700670 GEO Accession GSM1700670 SRX1044134 GSM1700671 SRP058873 SRS949619 GSM1700671 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700671 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700671 gds 301700671 GEO Accession GSM1700671 SRX1044135 GSM1700672 SRP058873 SRS949618 GSM1700672 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700672 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700672 gds 301700672 GEO Accession GSM1700672 SRX1044144 GSM1700681 SRP058873 SRS949609 GSM1700681 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700681 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700681 gds 301700681 GEO Accession GSM1700681 SRX1044145 GSM1700682 SRP058873 SRS949608 GSM1700682 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700682 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700682 gds 301700682 GEO Accession GSM1700682 SRX1044146 GSM1700683 SRP058873 SRS949607 GSM1700683 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700683 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700683 gds 301700683 GEO Accession GSM1700683 SRX1044147 GSM1700684 SRP058873 SRS949606 GSM1700684 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700684 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700684 gds 301700684 GEO Accession GSM1700684 SRX1044148 GSM1700685 SRP058873 SRS949605 GSM1700685 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700685 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700685 gds 301700685 GEO Accession GSM1700685 SRX1044149 GSM1700686 SRP058873 SRS949604 GSM1700686 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700686 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700686 gds 301700686 GEO Accession GSM1700686 SRX1044150 GSM1700687 SRP058873 SRS949602 GSM1700687 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700687 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700687 gds 301700687 GEO Accession GSM1700687 SRX1044151 GSM1700688 SRP058873 SRS949603 GSM1700688 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700688 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700688 gds 301700688 GEO Accession GSM1700688 SRX1044152 GSM1700689 SRP058873 SRS949601 GSM1700689 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700689 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700689 gds 301700689 GEO Accession GSM1700689 SRX1044153 GSM1700690 SRP058873 SRS949600 GSM1700690 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700690 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700690 gds 301700690 GEO Accession GSM1700690 SRX1044154 GSM1700691 SRP058873 SRS949599 GSM1700691 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700691 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700691 gds 301700691 GEO Accession GSM1700691 SRX1044155 GSM1700692 SRP058873 SRS949598 GSM1700692 MNase-Seq GENOMIC MNase In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700692 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700692 gds 301700692 GEO Accession GSM1700692 SRX1044164 GSM1700701 SRP058873 SRS949590 GSM1700701 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700701 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700701 gds 301700701 GEO Accession GSM1700701 SRX1044165 GSM1700702 SRP058873 SRS949588 GSM1700702 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700702 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700702 gds 301700702 GEO Accession GSM1700702 SRX1044166 GSM1700703 SRP058873 SRS949587 GSM1700703 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700703 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700703 gds 301700703 GEO Accession GSM1700703 SRX1044167 GSM1700704 SRP058873 SRS949585 GSM1700704 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700704 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700704 gds 301700704 GEO Accession GSM1700704 SRX1044171 GSM1700711 SRP058873 SRS949582 GSM1700711 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700711 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700711 gds 301700711 GEO Accession GSM1700711 SRX1044172 GSM1700712 SRP058873 SRS949581 GSM1700712 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700712 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700712 gds 301700712 GEO Accession GSM1700712 SRX1044173 GSM1700713 SRP058873 SRS949580 GSM1700713 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700713 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700713 gds 301700713 GEO Accession GSM1700713 SRX1044174 GSM1700714 SRP058873 SRS949578 GSM1700714 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700714 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700714 gds 301700714 GEO Accession GSM1700714 SRX1044175 GSM1700715 SRP058873 SRS949579 GSM1700715 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700715 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700715 gds 301700715 GEO Accession GSM1700715 SRX1044176 GSM1700716 SRP058873 SRS949577 GSM1700716 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700716 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700716 gds 301700716 GEO Accession GSM1700716 SRX1044177 GSM1700717 SRP058873 SRS949576 GSM1700717 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700717 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700717 gds 301700717 GEO Accession GSM1700717 SRX1044178 GSM1700718 SRP058873 SRS949575 GSM1700718 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700718 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700718 gds 301700718 GEO Accession GSM1700718 SRX1044179 GSM1700719 SRP058873 SRS949574 GSM1700719 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700719 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700719 gds 301700719 GEO Accession GSM1700719 SRX1044180 GSM1700720 SRP058873 SRS949573 GSM1700720 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700720 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700720 gds 301700720 GEO Accession GSM1700720 SRX1044181 GSM1700721 SRP058873 SRS949572 GSM1700721 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700721 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700721 gds 301700721 GEO Accession GSM1700721 SRX1044182 GSM1700722 SRP058873 SRS949571 GSM1700722 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700722 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700722 gds 301700722 GEO Accession GSM1700722 SRX1044183 GSM1700723 SRP058873 SRS949570 GSM1700723 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700723 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700723 gds 301700723 GEO Accession GSM1700723 SRX1044184 GSM1700724 SRP058873 SRS949569 GSM1700724 ChIP-Seq GENOMIC ChIP In MNase-seq experiments, nuclei were prepared from unfixed yeast cells and then digested with Mnase. Mono-nucleosomal DNA was gel-purified (~150 bp). See paper for details. In ChIP-seq experiments, cells were formaldehyde cross-linked before harvasting (see methods for details). The DNA was repaired using the DNA repair kit from New England Biolabs. The repaired DNA was processed for paired-end sequencing according to the Illumina protocol. Illumina HiSeq 2000 GEO Sample GSM1700724 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1700724 gds 301700724 GEO Accession GSM1700724