A very clear and informative tutorial. Just to add that the latest version of the peak caller (MACS2) specifically handles paired-end mapped reads. This results in a more accurate estimation of the mean DNA fragment size that can lead to a better estimation of the peak summit.
Thanks, explain the overall workflow very well. Just wondering if anyone has any recommendations about a tutorial that explains everything in terms of the command-line/ programming environment so that we can plot whatever we want.
You can try making use of the Biostar Handbook_2nd edition by Dr. Istvan Albert. It contains practical guide into the command line/programing environment using different OS as case study. All the best.
A very clear and informative tutorial. Just to add that the latest version of the peak caller (MACS2) specifically handles paired-end mapped reads. This results in a more accurate estimation of the mean DNA fragment size that can lead to a better estimation of the peak summit.
Extremely helpful and detailed introduction to sequencing! Thank you.
thank you for this great presentation!
Very clear, practical and informative.
Very informative, thank you
Thank you. It is exactly what I need.
amazing tutorial
Thank you so much for this tutorial
Thanks, explain the overall workflow very well. Just wondering if anyone has any recommendations about a tutorial that explains everything in terms of the command-line/ programming environment so that we can plot whatever we want.
You can try making use of the Biostar Handbook_2nd edition by Dr. Istvan Albert. It contains practical guide into the command line/programing environment using different OS as case study. All the best.
THANK YOU, Thank You, Thank you, thank you
Hello, How do you normalized the Chip-seq samples? thanks
thank you!
Can anyone link me to the fastq files used here?