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Website: Earray.chem.agilent.com
Hostname: earray.chem.agilent.com
Region: CA
City: Santa Clara
Postal Code: 95051
Latitude: 37.350101470947
Longitude: -121.98539733887
Area Code: 408
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Found 46 Websites with content related to this domain, It is result after search with search engine

Agilent Technologies

(3 day ago) Guest View | Login Page | Help


DA: 23 PA: 8 MOZ Rank: 31


(4 day ago) eArray 6.5 – Overview (1) : earray portal Li Login : [email protected] l [email protected] Password : assises2010 Agilent Restricted Confidentiality Label July 9, 20103


DA: 15 PA: 49 MOZ Rank: 64

Epigenetic & Location Analysis Microarrays | Agilent

(9 day ago) Discover our selection of Location Analysis Microarrays for your experiments. Our range of high-performing microarrays include catalog and custom ChIP-on-chip and DNA Methylation Microarrays. Our CpG Microarrays enable insights into the DNA methylation changes that may be correlated to key biological processes. Learn more


DA: 15 PA: 50 MOZ Rank: 50

ISCA SurePrint Microarrays - chem-agilent.com

(22 day ago) Visit: https://earray.chem.agilent.com CGH probes and SNP probes on one microarray! 180K Agilent 180K 180K 180K 180K Agilent 60K 60K 60K 60K 60K 60K 60K 60K Agilent 105K 105K Agilent 44K 44K 44K 44K Agilent


DA: 20 PA: 23 MOZ Rank: 43

Breakpoint junction analysis for complex genomic

(1 month ago) Chromosomal triplications can be classified into recurrent and nonrecurrent triplications. Most of the nonrecurrent triplications are embedded in duplicated segments, and duplication‐inverted triplication–duplication (DUP–TRP/INV‐DUP) has been established as one of the mechanisms of triplication.


DA: 23 PA: 23 MOZ Rank: 46

Agilent Technologies Page 1 of 6

(1 month ago) pr int terms and conditions governing agilent's earray program attention: this site is provided subject to these terms and conditions. please


DA: 20 PA: 29 MOZ Rank: 49

Multi‐gene panel testing improves - Wiley Online Library

(9 day ago) Mutations in more than 70 genes cause hereditary anemias (HA), a highly heterogeneous group of rare/low frequency disorders in which we included: hyporegenerative anemias, as congenital dyserythropoietic anemia (CDA) and Diamond‐Blackfan anemia; hemolytic anemias due to erythrocyte membrane defects, as hereditary spherocytosis and stomatocytosis; hemolytic anemias due to enzymatic defects.


DA: 23 PA: 27 MOZ Rank: 50

Bed For Agilent Sureselect All Exon Kits

(1 day ago) I can confirm that, 5 years later, this solution still works. I had to create an account at suredesign, then click "find designs", then click "agilent catalog", then you get to a list of a bunch of sureselect kits with download links including .bed files.


DA: 16 PA: 9 MOZ Rank: 25

Appropriate bed files from library capture kit for

(5 day ago) I'm not sure how typical this situation is, where the Covered and Regions files are exactly the same intervals. In case it is not the norm, I am supplementing the response from finswimmer with a couple old posts for reference.. I use this prior post for reference on what the different Agilent bed files contain: Question: Human Exome Capture Library Coordinates Download


DA: 16 PA: 10 MOZ Rank: 26

Prioritization and burden analysis of rare variants in 208

(22 day ago) The most common cause of end-stage renal disease in children is attributed to congenital anomalies of the kidney and urinary tract (CAKUT).1, 2 CAKUT refers to structural malformations of the kidneys (renal agenesis, hypoplasia, dysplasia, duplex collecting system) and abnormalities of the ureter and urethra (uretero–pelvic junction obstruction and posterior urethral valves).


DA: 21 PA: 38 MOZ Rank: 59

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