mirgator kobic.re.kr

miRGator3.0

A microRNA portal in deep sequencing era. 1 miR-seq browser . MiR-seq browser that visualizes the sequence alignment and normalized read counts with the secondary structure information simultaneously in concurrent windows. Short reads related to iso-miRs and miRNA editing can be readily identified with the corresponding expression values read counts in multiple samples. This helps users to easily examine the relationships between the structure of precursor, the sequences and abundance of fina.MiRNA.

OVERVIEW

The web site mirgator.kobic.re.kr currently has an average traffic classification of zero (the smaller the higher page views).

MIRGATOR.KOBIC.RE.KR TRAFFIC

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WHAT DOES MIRGATOR.KOBIC.RE.KR LOOK LIKE?

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MIRGATOR.KOBIC.RE.KR SERVER

Our crawlers observed that a lone root page on mirgator.kobic.re.kr took eight hundred and fifty-nine milliseconds to stream. I could not detect a SSL certificate, so our parsers consider mirgator.kobic.re.kr not secure.
Load time
0.859 sec
SSL
NOT SECURE
IP
210.218.222.211

SERVER SOFTWARE AND ENCODING

We found that this website is employing the Apache-Coyote/1.1 os.

SITE TITLE

miRGator3.0

DESCRIPTION

A microRNA portal in deep sequencing era. 1 miR-seq browser . MiR-seq browser that visualizes the sequence alignment and normalized read counts with the secondary structure information simultaneously in concurrent windows. Short reads related to iso-miRs and miRNA editing can be readily identified with the corresponding expression values read counts in multiple samples. This helps users to easily examine the relationships between the structure of precursor, the sequences and abundance of fina.MiRNA.

PARSED CONTENT

The web site mirgator.kobic.re.kr has the following in the site, "A microRNA portal in deep sequencing era." I noticed that the webpage also stated " MiR-seq browser that visualizes the sequence alignment and normalized read counts with the secondary structure information simultaneously in concurrent windows." They also said " Short reads related to iso-miRs and miRNA editing can be readily identified with the corresponding expression values read counts in multiple samples. This helps users to easily examine the relationships between the structure of precursor, the sequences and abundance of fina."

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