Fios Genomics

@fiosgenomics

Supporting small to big pharma and biotechs in their data analysis needs. Providing a wide range of bioinformatics services for drug discovery & development.

Edinburgh, Scotland
fiosgenomics.com
ಜೂನ್ 2011 ಸಮಯದಲ್ಲಿ ಸೇರಿದ್ದಾರೆ
572 ಫೋಟೋಗಳು ಅಥವಾ ವೀಡಿಯೋಗಳು ಫೋಟೋಗಳು ಮತ್ತು ವೀಡಿಯೋಗಳು

ಟ್ವೀಟ್‌ಗಳು

ನೀವು @fiosgenomics ಅವರನ್ನು ತಡೆಹಿಡಿದಿರುವಿರಿ

ಈ ಟ್ವೀಟ್‌ಗಳನ್ನು ವೀಕ್ಷಿಸಲು ನೀವು ಖಚಿತವಾಗಿ ಬಯಸುವಿರಾ? ಟ್ವೀಟ್ ವೀಕ್ಷಣೆಯು @fiosgenomics ಅವರ ತಡೆತೆರವುಗೊಳಿಸುವುದಿಲ್ಲ

  1. ಡಿಸೆಂ 18

    The work we do often goes into publications and posters - have a look at some of the posters our work has been featured on, as well as case studies we've produced.

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  2. ಡಿಸೆಂ 17

    We're hiring! We're looking for an additional bioinformatics team leader to join our growing team - to find out more about the opportunity, visit:

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  3. ಡಿಸೆಂ 15

    Fundamental differences between cancerous and normal genomes have led to the 'Methylscape' - a universal biomarker displayed by most cancers. This allows for an analysis time of <10 minutes to detect many cancer types. Read the full paper in :

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  4. ಡಿಸೆಂ 13

    Fios have had a busy 2018 - catch up with all our achievements and highlights in our round up blog post now!

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  5. ಡಿಸೆಂ 10

    Wondering who's on our team? Meet the Fios key contacts - from our CEO to project manager, find out more about some of the people that work at Fios!

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  6. ಡಿಸೆಂ 8

    Part of the club! New paper in has shown paternal mitochondria can be transmitted along with maternal. This "profoundly alters a widespread belief about mitochondrial inheritance and potentially opens a novel field in mitochondrial medicine."

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  7. ಡಿಸೆಂ 6

    With less than four weeks left of 2018, our roundup newsletter for the year is coming out next week! Don't miss out - if you want to receive it, sign up now:

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  8. ಡಿಸೆಂ 4

    Genome sequencing is hugely important - and as it becomes faster and cheaper to do, more organisms are having their entire genome sequenced. Take a brief look at some organisms that have been sequenced in our new blog post -

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  9. ಡಿಸೆಂ 2

    How much has changed in nearly 20 years - in 1999, the longest stretch of DNA was decoded. Chromosome 22, over 23 million letters long, was sequenced using overlapping cloned segments of DNA. Now, whole genome sequencing can take as little time as a day.

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  10. ನವೆಂ 29

    Diversity in sequenced genomes is important - sequencing >900 individuals of African descent highlighted ~300 million base pairs in 126,000 distinct contigs not present in reference genome. African pan-genome has ~10% more DNA compared to current reference

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  11. ನವೆಂ 26

    Wanting to dive deeper into data you've already produced? Maybe your research is looking into a publically available dataset? We can help - our data mining solutions will help you get the best answers to your research questions. Find out more today:

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  12. ನವೆಂ 24

    Using NGS to sequence the domestic turkey: combining two sequencing platforms, >15,000 protein coding genes were identified. Turkey genome helps understand the evolution of economically valuable traits seen in poultry. Read the full paper in PLOS Biology:

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  13. ನವೆಂ 22

    Wishing all our US clients and connections a happy Thanksgiving today!

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  14. ನವೆಂ 20

    The first step's always the hardest - true for experiments too. A well designed and set-up study allows for interpretable results at the data analysis stage. It also reduces issues further down your pipeline. Read the new post on experimental design now:

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  15. ನವೆಂ 17

    Finding where a genetic disease is located on a chromosome is the first step to finding its underlying cause. In 1983, Huntington’s Disease was mapped onto chromosome 4 – it took another 10 years for the genetic sequence to be isolated.

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  16. ನವೆಂ 16

    Clincial trials to allow for more optimised drug treatments? A recent paper reviews using new biomarkers for genomic analysis to reduce resistance and relapse rates in cancer patients.

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  17. ನವೆಂ 15

    Excited to be at the BioCity today with who are keen to talk about building a network of companies and CROs able to provide drug discovery expertise and services.

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  18. ಅವರು ಮರುಟ್ವೀಟಿಸಿದ್ದಾರೆ
    ನವೆಂ 14

    There may be five kinds of diabetes, not just types 1 and 2 (free to read for )

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  19. ನವೆಂ 12

    It's only been a month since - the programme production by and - was released! Find out more about how Fios, as a bioinformatics provider, helps to extract meaningful information from complex datasets.

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  20. ನವೆಂ 10

    Metabolomics provides new insights into diseases e.g. cancer. Many conditions affect brain metabolic processes, but there's a lack of study into the tumour brain metabolome. Tumour growth & neurodegenerative disease impact brain processes in similar ways.

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@fiosgenomics ಅವರು ಇನ್ನೂ ಟ್ವೀಟ್ ಮಾಡಿಲ್ಲ.

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