diff --git a/README.md b/README.md
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+++ b/README.md
@@ -5,6 +5,7 @@
 [![Nextflow](https://img.shields.io/badge/nextflow-%E2%89%A50.24.0-brightgreen.svg
 )](https://www.nextflow.io/)
 [![Astrocyte](https://img.shields.io/badge/astrocyte-%E2%89%A50.1.0-blue.svg)](https://astrocyte-test.biohpc.swmed.edu/static/docs/index.html)
+[![DOI](https://zenodo.org/badge/DOI/10.5281/zenodo.2648845.svg)](https://doi.org/10.5281/zenodo.2648845)
 
 
 ## Introduction
diff --git a/docs/index.md b/docs/index.md
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+++ b/docs/index.md
@@ -1,4 +1,4 @@
-# Astrocyte ChIPseq analysis Workflow Package
+# BICF ChIP-seq Analysis Workflow
 
 ## Introduction
 **ChIP-seq Analysis** is a bioinformatics best-practice analysis pipeline used for chromatin immunoprecipitation (ChIP-seq) data analysis.
@@ -7,16 +7,16 @@ The pipeline uses [Nextflow](https://www.nextflow.io), a bioinformatics workflow
 
 ### Pipeline Steps
 
-1) Trim adaptors TrimGalore!
-2) Align with BWA
-3) Filter reads with Sambamba  S
-4) Quality control with DeepTools
-5) Calculate Cross-correlation using SPP and PhantomPeakQualTools
-6) Signal profiling using MACS2
-7) Call consenus peaks
-8) Annotate all peaks using ChipSeeker
-9) Use MEME-ChIP to find motifs in original peaks
-10) Find differential expressed peaks using DiffBind (If more than 1 experiment)
+  1) Trim adaptors TrimGalore!
+  2) Align with BWA
+  3) Filter reads with Sambamba  S
+  4) Quality control with DeepTools
+  5) Calculate Cross-correlation using SPP and PhantomPeakQualTools
+  6) Signal profiling using MACS2
+  7) Call consenus peaks
+  8) Annotate all peaks using ChipSeeker
+  9) Use MEME-ChIP to find motifs in original peaks
+  10) Find differential expressed peaks using DiffBind (If more than 1 experiment)
 
 
 ## Workflow Parameters
@@ -25,41 +25,35 @@ The pipeline uses [Nextflow](https://www.nextflow.io), a bioinformatics workflow
     pairedEnd - Choose True/False if data is paired-end
     design - Choose the file with the experiment design information. TSV format
     genome - Choose a genomic reference (genome).
+    skipDiff - Choose True/False if data if you want to run Differential Peaks
+    skipMotif - Choose True/False if data if you want to run Motif Calling
 
 
 ## Design file
 
- The following columns are necessary, must be named as in template. An design file template can be downloaded [HERE](https://git.biohpc.swmed.edu/bchen4/chipseq_analysis/raw/master/docs/design_example.csv)
-
-    SampleID
-        The id of the sample. This will be the header in output files, please make sure it is concise
-    Tissue
-        Tissue of the sample
-    Factor
-        Factor of the experiment
-    Condition
-	    This is the group that will be used for pairwise differential expression analysis
-	Replicate
-	    Replicate id
-    Peaks
-        The file name of the peak file for this sample
-    bamReads
-        The file name of the IP BAM for this sample
-    bamControl
-        The file name of the control BAM for this sample
-    ContorlID
-        The id of the control sample
-    PeakCaller
-        The peak caller used
-
+ The following columns are necessary, must be named as in template. An design file template can be downloaded [HERE](https://git.biohpc.swmed.edu/BICF/Astrocyte/chipseq_analysis/blob/master/docs/design_example.txt)
+
+    sample_id
+        The id of the sample. This will be the name used in output files, please make sure it is concise and informative.
+    experiment_id
+        The id of the experiment. Used for grouping replicates.
+    biosample
+        The name of the biological sample.
+    factor
+        Factor of the experiment.
+    treatment
+        Treatment used in experiment.
+    replicate
+        Replicate number.
+    control_id
+	    The sample_id of the control used for this sample.
+    fastq_read1
+      File name of fastq file, if paired-end this is read1.
+    fastq_read2
+      File name of read2 (for paired-end), not needed for single-end data.
 
 
 ### Credits
-This example worklow is derived from original scripts kindly contributed by the Bioinformatic Core Facility (BICF), Department of Bioinformatics
-
-### References
+This worklow is was developed jointly with the [Bioinformatic Core Facility (BICF), Department of Bioinformatics](http://www.utsouthwestern.edu/labs/bioinformatics/)
 
-* ChipSeeker: http://bioconductor.org/packages/release/bioc/html/ChIPseeker.html
-* DiffBind: http://bioconductor.org/packages/release/bioc/html/DiffBind.html
-* Deeptools: https://deeptools.github.io/
-* MEME-ChIP: http://meme-suite.org/doc/meme-chip.html
+Please cite in publications: Pipeline was developed by BICF from funding provided by **Cancer Prevention and Research Institute of Texas (RP150596)**.
diff --git a/docs/references.md b/docs/references.md
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+++ b/docs/references.md
@@ -50,3 +50,8 @@
 
 16. **MultiQc**:
   * Ewels P., Magnusson M., Lundin S. and Käller M. 2016. MultiQC: Summarize analysis results for multiple tools and samples in a single report. Bioinformatics 32(19): 3047–3048. doi:[10.1093/bioinformatics/btw354 ](https://dx.doi.org/10.1093/bioinformatics/btw354)
+
+17. **BICF ChIP-seq Analysis Workflow**:
+  * Venkat S. Malladi and Beibei Chen. (2019). BICF ChIP-seq Analysis Workflow (publish_1.0.0). Zenodo. doi:[10.5281/zenodo.2648845](https://doi.org/10.5281/zenodo.2648845)
+
+Please cite in publications: Pipeline was developed by BICF from funding provided by **Cancer Prevention and Research Institute of Texas (RP150596)**.