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on page 1 showing 20 out of 3,231,408 results from 4 sources

Cite this (AGSC Cat# 100A, RRID:AGSC_100A)

Source Database: AGSC, catalog # 100A
Genetic Background:
Affected Genes:
Genomic Alteration:
Availability: live
Reference:
Notes: wild-type Size: adults


https://web.expasy.org/cellosaurus/CVCL_C252

Cite this: (ATCC Cat# ACS-1003, RRID:CVCL_C252)
Organism: Homo sapiens
Disease: Down syndrome
Category: Induced pluripotent stem cell
Comment:


http://antibodyregistry.org/AB_2314273

Cite this (21st Century Biochemicals Cat# Clark et al 2008, RRID:AB_2314273)
Comments:
References: PMID:19941347
Host Organism:
Clonality: unknown
Target(s):


    (at)Note

Cite this ((at)Note, RRID:SCR_005342)

URL: http://darwin.di.uminho.pt/anote2/wiki/index.php/Main_Page

Resource Type: Resource, software resource, software application, text-mining software

THIS RESOURCE IS NO LONGER AVAILABLE. Documented September 18, 2017

Text Mining platform that copes with major Information Retrieval and Information Extraction tasks and promotes multi-disciplinary research. It aims to provide support to three different usage roles: biologists, text miners and application developers. The workbench supports the retrieval, processing and annotation of documents as well as their analysis at different levels.


Cite this (AGSC Cat# 100E, RRID:AGSC_100E)

Source Database: AGSC, catalog # 100E
Genetic Background:
Affected Genes:
Genomic Alteration:
Availability: live
Reference:
Notes: wild-type Size: embryos


https://web.expasy.org/cellosaurus/CVCL_C250

Cite this: (ATCC Cat# ACS-1004, RRID:CVCL_C250)
Organism: Homo sapiens
Disease: Cystic fibrosis
Category: Induced pluripotent stem cell
Comment: Sequence variation: Homozygous for CFTR p.Phe508del (ATCC).


http://antibodyregistry.org/AB_1645968

Cite this (3H Biomedical AB Cat# 3HANT 101, RRID:AB_1645968)
Comments: manufacturer recommendations:
References:
Host Organism: mouse
Clonality: unknown
Target(s): HA-tag peptide


Cite this (100, 000 Genomes Project, RRID:SCR_010502)

URL: http://www.genomicsengland.co.uk/the-100000-genomes-project/

Resource Type: Resource, data or information resource, database

The project will focus on patients with a rare disease and their families and patients with cancer. The first samples for sequencing are being taken from patients living in England with discussions taking place with Scotland, Wales and Northern Ireland about potential future involvement. Genomics England, a company wholly owned and funded by the Department of Health, was set up to deliver this flagship project which will sequence 100,000 whole genomes from NHS patients by 2017. Its four main aims are; to create an ethical and transparent programme based on consent; to bring benefit to patients and set up a genomic medicine service for the NHS; to enable new scientific discovery and medical insights; and to kick start the development of a UK genomics industry.


Cite this (AGSC Cat# 100H, RRID:AGSC_100H)

Source Database: AGSC, catalog # 100H
Genetic Background:
Affected Genes:
Genomic Alteration:
Availability: live
Reference:
Notes: wild-type Size: hatchlings


https://web.expasy.org/cellosaurus/CVCL_C256

Cite this: (ATCC Cat# ACS-1007, RRID:CVCL_C256)
Organism: Homo sapiens
Disease:
Category: Induced pluripotent stem cell
Comment:


http://antibodyregistry.org/AB_1646004

Cite this (3H Biomedical AB Cat# 3HANT 102, RRID:AB_1646004)
Comments: manufacturer recommendations:
References:
Host Organism: mouse
Clonality: unknown
Target(s): Human Interleukin-2


Cite this (1000 Functional Connectomes Project, RRID:SCR_005361)

URL: http://fcon_1000.projects.nitrc.org/

Resource Type: Resource, database, image collection, catalog, service resource, storage service resource, image repository, data repository, data or information resource

Database of resting state fMRI (R-fMRI) datasets collected from sites around the world. It demonstrates open sharing of R-fMRI data and aims to emphasize the aggregation and sharing of well-phenotyped datasets.


Cite this (AGSC Cat# 100J, RRID:AGSC_100J)

Source Database: AGSC, catalog # 100J
Genetic Background:
Affected Genes:
Genomic Alteration:
Availability: live
Reference:
Notes: wild-type Size: juveniles


https://web.expasy.org/cellosaurus/CVCL_C253

Cite this: (ATCC Cat# ACS-1011, RRID:CVCL_C253)
Organism: Homo sapiens
Disease:
Category: Induced pluripotent stem cell
Comment:


http://antibodyregistry.org/AB_1646007

Cite this (3H Biomedical AB Cat# 3HANT 103, RRID:AB_1646007)
Comments: manufacturer recommendations:
References:
Host Organism: rat
Clonality: unknown
Target(s): Mouse Interleukin-2 receptor


Cite this (1000 Genomes: A Deep Catalog of Human Genetic Variation, RRID:SCR_006828)

URL: http://www.1000genomes.org/

Resource Type: Resource, organization portal, database, consortium, data set, portal, data or information resource

International collaboration producing an extensive public catalog of human genetic variation, including SNPs and structural variants, and their haplotype contexts, in an effort to provide a foundation for investigating the relationship between genotype and phenotype. The genomes of about 2500 unidentified people from about 25 populations around the world were sequenced using next-generation sequencing technologies. Redundant sequencing on various platforms and by different groups of scientists of the same samples can be compared. The results of the study are freely and publicly accessible to researchers worldwide. The consortium identified the following populations whose DNA will be sequenced: Yoruba in Ibadan, Nigeria; Japanese in Tokyo; Chinese in Beijing; Utah residents with ancestry from northern and western Europe; Luhya in Webuye, Kenya; Maasai in Kinyawa, Kenya; Toscani in Italy; Gujarati Indians in Houston; Chinese in metropolitan Denver; people of Mexican ancestry in Los Angeles; and people of African ancestry in the southwestern United States. The goal Project is to find most genetic variants that have frequencies of at least 1% in the populations studied. Sequencing is still too expensive to deeply sequence the many samples being studied for this project. However, any particular region of the genome generally contains a limited number of haplotypes. Data can be combined across many samples to allow efficient detection of most of the variants in a region. The Project currently plans to sequence each sample to about 4X coverage; at this depth sequencing cannot provide the complete genotype of each sample, but should allow the detection of most variants with frequencies as low as 1%. Combining the data from 2500 samples should allow highly accurate estimation (imputation) of the variants and genotypes for each sample that were not seen directly by the light sequencing. All samples from the 1000 genomes are available as lymphoblastoid cell lines (LCLs) and LCL derived DNA from the Coriell Cell Repository as part of the NHGRI Catalog. The sequence and alignment data generated by the 1000genomes project is made available as quickly as possible via their mirrored ftp sites. ftp://ftp.1000genomes.ebi.ac.uk ftp://ftp-trace.ncbi.nlm.nih.gov/1000genomes


Cite this (AGSC Cat# 100L, RRID:AGSC_100L)

Source Database: AGSC, catalog # 100L
Genetic Background:
Affected Genes:
Genomic Alteration:
Availability: live
Reference:
Notes: wild-type Size: larvae


https://web.expasy.org/cellosaurus/CVCL_C254

Cite this: (ATCC Cat# ACS-1012, RRID:CVCL_C254)
Organism: Homo sapiens
Disease: Parkinson's disease
Category: Induced pluripotent stem cell
Comment:


http://antibodyregistry.org/AB_1646006

Cite this (3H Biomedical AB Cat# 3HANT 104, RRID:AB_1646006)
Comments: manufacturer recommendations:
References:
Host Organism: mouse
Clonality: unknown
Target(s): Human Interleukin-2 receptor


Cite this (1000 Genomes Project and AWS, RRID:SCR_008801)

URL: http://aws.amazon.com/1000genomes/

Resource Type: Resource, data set, data or information resource

A dataset containing the full genomic sequence of 1,700 individuals, freely available for research use. The 1000 Genomes Project is an international research effort coordinated by a consortium of 75 companies and organizations to establish the most detailed catalogue of human genetic variation. The project has grown to 200 terabytes of genomic data including DNA sequenced from more than 1,700 individuals that researchers can now access on AWS for use in disease research free of charge. The dataset containing the full genomic sequence of 1,700 individuals is now available to all via Amazon S3. The data can be found at: http://s3.amazonaws.com/1000genomes The 1000 Genomes Project aims to include the genomes of more than 2,662 individuals from 26 populations around the world, and the NIH will continue to add the remaining genome samples to the data collection this year. Public Data Sets on AWS provide a centralized repository of public data hosted on Amazon Simple Storage Service (Amazon S3). The data can be seamlessly accessed from AWS services such Amazon Elastic Compute Cloud (Amazon EC2) and Amazon Elastic MapReduce (Amazon EMR), which provide organizations with the highly scalable compute resources needed to take advantage of these large data collections. AWS is storing the public data sets at no charge to the community. Researchers pay only for the additional AWS resources they need for further processing or analysis of the data. All 200 TB of the latest 1000 Genomes Project data is available in a publicly available Amazon S3 bucket. You can access the data via simple HTTP requests, or take advantage of the AWS SDKs in languages such as Ruby, Java, Python, .NET and PHP. Researchers can use the Amazon EC2 utility computing service to dive into this data without the usual capital investment required to work with data at this scale. AWS also provides a number of orchestration and automation services to help teams make their research available to others to remix and reuse. Making the data available via a bucket in Amazon S3 also means that customers can crunch the information using Hadoop via Amazon Elastic MapReduce, and take advantage of the growing collection of tools for running bioinformatics job flows, such as CloudBurst and Crossbow.


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