From e34e7da50fc0ff5ed41e8bdaf2b1d41c9e9cf534 Mon Sep 17 00:00:00 2001 From: Bonface Date: Thu, 15 Feb 2024 06:09:54 -0600 Subject: Update dataset RTF Files. --- .../HQFNeoc_0208_RankInv/acknowledgment.rtf | 6 - general/datasets/HQFNeoc_0208_RankInv/cases.rtf | 54 -- .../HQFNeoc_0208_RankInv/experiment-design.rtf | 937 --------------------- general/datasets/HQFNeoc_0208_RankInv/platform.rtf | 7 - .../datasets/HQFNeoc_0208_RankInv/processing.rtf | 3 - general/datasets/HQFNeoc_0208_RankInv/summary.rtf | 16 - general/datasets/HQFNeoc_0208_RankInv/tissue.rtf | 9 - 7 files changed, 1032 deletions(-) delete mode 100644 general/datasets/HQFNeoc_0208_RankInv/acknowledgment.rtf delete mode 100644 general/datasets/HQFNeoc_0208_RankInv/cases.rtf delete mode 100644 general/datasets/HQFNeoc_0208_RankInv/experiment-design.rtf delete mode 100644 general/datasets/HQFNeoc_0208_RankInv/platform.rtf delete mode 100644 general/datasets/HQFNeoc_0208_RankInv/processing.rtf delete mode 100644 general/datasets/HQFNeoc_0208_RankInv/summary.rtf delete mode 100644 general/datasets/HQFNeoc_0208_RankInv/tissue.rtf (limited to 'general/datasets/HQFNeoc_0208_RankInv') diff --git a/general/datasets/HQFNeoc_0208_RankInv/acknowledgment.rtf b/general/datasets/HQFNeoc_0208_RankInv/acknowledgment.rtf deleted file mode 100644 index 3135d79..0000000 --- a/general/datasets/HQFNeoc_0208_RankInv/acknowledgment.rtf +++ /dev/null @@ -1,6 +0,0 @@ -
Data were generated with funds to RW Williams, Glenn D. Rosen, Weikuan Gu, and Lu Lu from the High Q Foundation. Informatics support also provided by NIH NIAAA INIA grants to RWW and LL.
- -The BXD genetic reference panel of recombinant inbred strains consists of just over 80 strains. The BXDs in this data set include 27 of the BXD strains made by Benjamin Taylor at the Jackson Laboratory in the 1970s and 1990s (BXD1 through BXD42). All of these strains are fully inbred, many well beyond the 100th filial (F) generation of inbreeding. We have also included 25 new inbred strains BXD (F21+) generated by Lu and Peirce. All of these strains were been genotyped at 13,377 SNPs in 2005 (Shifman et al., 2006).
- -Mouse Diversity Panel (MDP). We have profiled a MDP consisting 20 inbred strains and an F1 hybrid (B6D2F1). These strains were selected for several reasons:
- -All eight parents of the Collaborative Cross (129, A, C57BL/6J, CAST, NOD, NZO, PWK, and WSB) have been included in the MDP (noted below in the list). Twelve MDP strains have been sequenced, or are currently being resequenced by Perlegen for the NIEHS. This panel will be extremely helpful in systems genetic analysis of a wide variety of traits, and will be a powerful adjunct in fine mapping modulators using what is essentially an association analysis of sequence variants.
- -These strains are available from The Jackson Laboratory. BXD43 through BXD100 strains are available from Lu Lu and colleagues at UTHSC.
diff --git a/general/datasets/HQFNeoc_0208_RankInv/experiment-design.rtf b/general/datasets/HQFNeoc_0208_RankInv/experiment-design.rtf deleted file mode 100644 index 322268a..0000000 --- a/general/datasets/HQFNeoc_0208_RankInv/experiment-design.rtf +++ /dev/null @@ -1,937 +0,0 @@ -This data set consists arrays processed in XX groups over a XX month period (from Month Year to Month Year). Most groups consisted of XX samples. All arrays in this data set were processed using a single protocol by a single operator, NAME HERE. Processing was supervised directly by Dr. Lu Lu. All samples were scanned on a single Illumina Beadstation housed in the Hamilton Eye Institute between Month Day and Month Day, Year. Details on sample assignment to slides and batches is provide in the table below.
- -Error checking
- -Data Table 1:
- -This table lists all arrays by order of strain (index) and includes data on strain, sex, slide ID and slide position (A through F).
- -
-
|
-
Illumina Sentrix Mouse-6.1 BeadArray Platform (ILM6v1.1): The Mouse6.1 array consists of 46,643 unique probe sequences, each 50 nucleotides in length, that have been arrayed on glass slides using a novel bead technology.
- -Dunning M, Smith M, Thorne N, Tavare S (2006) beadarray: An R package to analyse Illumina BeadArrays. R News (the Newsletter of the P Project) 6:17-23. (see pages 17-23 of http://CRAN.R-project.org/doc/Rnews/Rnews_2006-5.pdf).
- -ANNOTATION: In summer of 2008, Xusheng Wang and Robert W. Williams reannotated the Illumina Mouse-6.1 array content. This new annotation is now incorporated into GeneNetwork. For 46643 probes on the Mouse 6.1 array platform (including control probes) we have identified XXXXX NCBI Entrez Gene IDs; XXXXX matched human Gene IDs; XXXXX matched rat Gene IDs; XXXXX NCBI HomoloGene IDs; and XXXXX OMIM IDs.
- -Position data for the 50-mer Illumina Mouse-6 array were initially downloaded from Sanger at http://www.sanger.ac.uk/Users/avc/Illumina/Mouse-6_V1.gff.gz but we then updated all positions by BLAT analysis from mm6 positions to mm8 positions (Hongqiang Li).
diff --git a/general/datasets/HQFNeoc_0208_RankInv/processing.rtf b/general/datasets/HQFNeoc_0208_RankInv/processing.rtf deleted file mode 100644 index 895fa91..0000000 --- a/general/datasets/HQFNeoc_0208_RankInv/processing.rtf +++ /dev/null @@ -1,3 +0,0 @@ -This data set uses the standard Rank Invariant method developed by Illumina and described in their BeadStation Studio documentation.
- -Sex of the samples was validated using sex-specific probe set: Xist probe ILM104280446.
diff --git a/general/datasets/HQFNeoc_0208_RankInv/summary.rtf b/general/datasets/HQFNeoc_0208_RankInv/summary.rtf deleted file mode 100644 index ca42527..0000000 --- a/general/datasets/HQFNeoc_0208_RankInv/summary.rtf +++ /dev/null @@ -1,16 +0,0 @@ -The February 2008 High Q Foundation Neocortex data set provides estimates of mRNA expression in the cerebral cortex of 73 lines of mice, including 52 BXD strains, 20 standard inbred strains, and B6D2F1 isogenic hybrids. All samples are from normal adult control animals raised in a standard laboratory environment. All data were generated with funds provided by the High Q Foundation using the Illumina Mouse 6.1 bead array (the second version of the Illumina Mouse-6 platform).
- -While this February data release is still a provisional, we are not aware of any specific errors.
- -- -
A total of 129 pooled neocortex samples were processed using approximately XX Illumina Sentrix Mouse-6.1 oligomer microarray BeadArray slides. XX Mouse-6.1 slides and a total of 128 samples passed stringent quality control and error checking. This data set is a companion to the High Q Foundation Striatum data set and was processed using very closely matched methods and most of the same samples. This is our third large data set generated using the Illumina platform. This particular data set was processed using the Illumina "Rank Invariant" protocol. Values were log2 transformed and the current data range from XXX (very low or no expression) to XXXX (extremely high).
- -As a measure of data quality we often count the number of probes that are associated with LOD scores of greater than 10 (LRS > 46). In this Neocortex Illumina (Feb 08) RankInv data set, 1564 probes have LRS values >46 (LOD >10).
- -Users of these mouse neocortex data may also find the following complementary resources and papers useful:
- -All animals were raised at the Jackson Laboratory or at UTHSC in SPF facilities. All mice were killed by cervical dislocation. Whole brain dissections were performed at either Beth Israel Deaconess Medical Center by Glenn Rosen or at UTHSC by Lu Lu and colleagues. Neocortex samples were close to complete but are likely to include variable amounts of underlying white matter. Samples may also include parts of the pyriform cortex and subiculum.
- -A pool of dissected neocortical tissue from two to three naive adults of the same strain, sex, and age was collected in one session and used to generate RNA samples. The great majority (75%) of animals were sacrificed between 9:30 AM and 11:30 AM. All animals were sacrificed between 9 AM and 5 PM during the light phase. All RNA samples were extracted at UTHSC by Zhiping Jia (CHECK LAST STATEMENT WITH LU).
- -All animals used in this study were between XX and XX days of age (average of XX days; see Table 1 below). All animals were sacrifice between 9 AM and 5 PM during the light phase.
- -Sample Processing: Samples were processed by Lu Lu and colleagues in the Illumina Core at UTHSC between December 2007 and January 2008. All processing steps were performed by Feng Jiao. In brief, RNA purity was evaluated using the 260/280 nm absorbance ratio, and values had to be greater than 1.8 to pass our quality control (QC). The majority of samples had values between 1.9 and 2.1. RNA integrity was assessed using the Agilent Bioanalyzer 2100. The standard Eberwine T7 polymerase method was used to catalyze the synthesis of cDNA template from polyA-tailed RNA using the Ambion/Illumina (http://www.ambion.com/catalog/CatNum.php?AMIL1791) TotalPrep RNA amplication kit (Cat#IL1791). The biotin labeled cRNA was then evaluated using both the 260/280 ratio (values of 2.0-2.3 are acceptable) using a NanoDrop ND-1000 (http://www.nanodrop.com/nd-1000-overview.html). Those samples that passed QC steps (1-3% failed and new RNA samples had to be acquired and processed) were immediately used on Mouse-6 v 1.1 slide. The slides were hybridized and washed following standard Illumina protocols.
- -Replication and Sample Balance: We obtained a male sample pool and female sample pool from as many strains as possible. However, a number of strains are represented by samples from a single sex (see figure at bottom of page).
-- cgit v1.2.3