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  • *[[Using Bioconductor To Analyse Beadarray Data]] *[[Using Bioconductor To Analyse Microarray Data]]
    4 KB (484 words) - 12:10, 15 August 2016
  • #Analyse the data using [[Using Scrubber2 | Scrubber2]] and/or a separate analysis graphing p
    5 KB (753 words) - 14:40, 14 April 2011
  • ...ortcut to results”icon to open that window. Drag and drop the .sds (raw data) and .csv (Excel spreadsheet) files into the USB window. Right click on th
    3 KB (562 words) - 12:13, 28 May 2009
  • ...epared above to rescue the mice and prevent hypoglycmic shock. Ignore the data from this mouse from that point on. *Analyze data by both % change from fasting glucose and absolute values. Our preferred o
    4 KB (717 words) - 15:19, 7 March 2022
  • taken from [[http://www.signaling-gateway.org/data/cgi-bin/ProtocolFile.cgi/afcs_PP00000159.pdf?pid=PP00000159 Passage Procedu
    6 KB (860 words) - 15:28, 15 July 2009
  • Meta(gds) #show extracted meta data ...log=TRUE) #convert to expression set, by default obtains annotation (GPL) data with log2 transformation
    2 KB (354 words) - 15:34, 2 September 2009
  • **annotation data for the array (normally illuminaMousev2BeadID.db) ==Loading Data==
    5 KB (766 words) - 15:34, 2 September 2009
  • **annotation data for the array (normally either '''lumiMouseIDMapping''' or '''lumiHumanIDMa ==Loading Data==
    5 KB (722 words) - 15:34, 2 September 2009
  • *Under Data Channels change sample rate if required (10pts/s is usually OK). Click '''
    3 KB (484 words) - 19:22, 14 May 2010
  • *Data will be collected, saved and processed automatically.
    3 KB (455 words) - 18:38, 14 May 2010
  • #On the popup window select copy and paste the data into an excel document #On the popup window select copy and paste the data into an excel document
    752 bytes (136 words) - 13:42, 11 June 2010
  • #If there is pre-existing data in the database enter '''python manage.py migrate --fake''' to run a fake m
    628 bytes (86 words) - 19:39, 21 July 2010
  • #Go to setup and choose where to save your data.
    3 KB (559 words) - 19:47, 9 February 2011
  • ...are pre-built UCSC genomes and downloaded from ftp://ftp.cbcb.umd.edu/pub/data/bowtie_indexes/ ...enome in both .ebwt and fasta formats (e.g. /ccmb/CoreBA/BioinfCore/Common/DATA/BowtieData/H_Sapiens/hg19)> <reads file to be aligned (e.g. s_1_1_sequence.
    5 KB (760 words) - 16:08, 8 November 2011
  • ...or R for the analysis. To get data into R, the easiest way is to make the data in excel then import it into R with this command: * Using R, providing data is formatted in a dataframe named '''dataset''' with columns '''group''' an
    6 KB (1,029 words) - 18:10, 26 June 2012
  • # Check if the primer is available in the lab using the Primer Data sheet at https://docs.google.com/spreadsheets/d/1kQ1G52XuoqpAWHIWT5H2UDz4aD # Enter both primers in the Primer Data sheet used in Step 1
    1 KB (249 words) - 17:48, 29 June 2017
  • ==Data Processing==
    2 KB (250 words) - 14:57, 2 December 2013
  • * Present the data in glycerol (or FFA) released per hour per number of cells.
    2 KB (251 words) - 14:51, 11 November 2014
  • * Prepare a data sheet with one row per animal and space for 3-5 measurements per animal. * Record the peak grip on your data sheet
    1 KB (208 words) - 17:20, 14 February 2014
  • * Analyse data by both % change from fasting glucose and absolute values. You may also wa
    3 KB (461 words) - 17:50, 6 April 2022

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