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#pws — Public Fediverse posts

Live and recent posts from across the Fediverse tagged #pws, aggregated by home.social.

  1. According to my #PWS: 18 hour rainfall = 1.86" (47.24 mm)
    Southeastern Michigan

  2. Сначала Firebase, теперь Telegram. Как доставлять сборки, когда всё ломается?

    Привет! Меня зовут Владислав Лаптев, я директор по инновациям в Fork-Tech. Сегодня РБК выпустил материал о том, что замедление Telegram срывает релизы мобильных приложений в России. Мы дали комментарий для этого материала, и я решил рассказать подробнее, потому что проблема не в Telegram. Проблема в том, что российские мобильные разработчики третий раз за четыре года теряют инструмент доставки сборок. Мы создали PWS (Product Web Services) — платформу для управления цифровыми продуктами. Сегодня речь про модуль App Distribution: как мы к нему пришли, где взяли лучшее от Firebase, почему этого было мало, и как всё работает под капотом. С примерами кода из документации. Платформа включена в реестр российского ПО.

    habr.com/ru/articles/996014/

    #pws #android #ios #firebase #testflight #devops #telegram

  3. Сначала Firebase, теперь Telegram. Как доставлять сборки, когда всё ломается?

    Привет! Меня зовут Владислав Лаптев, я директор по инновациям в Fork-Tech. Сегодня РБК выпустил материал о том, что замедление Telegram срывает релизы мобильных приложений в России. Мы дали комментарий для этого материала, и я решил рассказать подробнее, потому что проблема не в Telegram. Проблема в том, что российские мобильные разработчики третий раз за четыре года теряют инструмент доставки сборок. Мы создали PWS (Product Web Services) — платформу для управления цифровыми продуктами. Сегодня речь про модуль App Distribution: как мы к нему пришли, где взяли лучшее от Firebase, почему этого было мало, и как всё работает под капотом. С примерами кода из документации. Платформа включена в реестр российского ПО.

    habr.com/ru/articles/996014/

    #pws #android #ios #firebase #testflight #devops #telegram

  4. Сначала Firebase, теперь Telegram. Как доставлять сборки, когда всё ломается?

    Привет! Меня зовут Владислав Лаптев, я директор по инновациям в Fork-Tech. Сегодня РБК выпустил материал о том, что замедление Telegram срывает релизы мобильных приложений в России. Мы дали комментарий для этого материала, и я решил рассказать подробнее, потому что проблема не в Telegram. Проблема в том, что российские мобильные разработчики третий раз за четыре года теряют инструмент доставки сборок. Мы создали PWS (Product Web Services) — платформу для управления цифровыми продуктами. Сегодня речь про модуль App Distribution: как мы к нему пришли, где взяли лучшее от Firebase, почему этого было мало, и как всё работает под капотом. С примерами кода из документации. Платформа включена в реестр российского ПО.

    habr.com/ru/articles/996014/

    #pws #android #ios #firebase #testflight #devops #telegram

  5. Сначала Firebase, теперь Telegram. Как доставлять сборки, когда всё ломается?

    Привет! Меня зовут Владислав Лаптев, я директор по инновациям в Fork-Tech. Сегодня РБК выпустил материал о том, что замедление Telegram срывает релизы мобильных приложений в России. Мы дали комментарий для этого материала, и я решил рассказать подробнее, потому что проблема не в Telegram. Проблема в том, что российские мобильные разработчики третий раз за четыре года теряют инструмент доставки сборок. Мы создали PWS (Product Web Services) — платформу для управления цифровыми продуктами. Сегодня речь про модуль App Distribution: как мы к нему пришли, где взяли лучшее от Firebase, почему этого было мало, и как всё работает под капотом. С примерами кода из документации. Платформа включена в реестр российского ПО.

    habr.com/ru/articles/996014/

    #pws #android #ios #firebase #testflight #devops #telegram

  6. I have successfully begun capturing my AcuRite Iris weather station data with an RTL-SDR antenna and the great open source software rtl_433. This is the first step in being able to actually use the measurements myself instead of just sending them all to The Weather Co for free.

    triq.org/rtl_433/

    #PWS

  7. I have successfully begun capturing my AcuRite Iris weather station data with an RTL-SDR antenna and the great open source software rtl_433. This is the first step in being able to actually use the measurements myself instead of just sending them all to The Weather Co for free.

    triq.org/rtl_433/

    #PWS

  8. I have successfully begun capturing my AcuRite Iris weather station data with an RTL-SDR antenna and the great open source software rtl_433. This is the first step in being able to actually use the measurements myself instead of just sending them all to The Weather Co for free.

    triq.org/rtl_433/

    #PWS

  9. I have successfully begun capturing my AcuRite Iris weather station data with an RTL-SDR antenna and the great open source software rtl_433. This is the first step in being able to actually use the measurements myself instead of just sending them all to The Weather Co for free.

    triq.org/rtl_433/

    #PWS

  10. I have successfully begun capturing my AcuRite Iris weather station data with an RTL-SDR antenna and the great open source software rtl_433. This is the first step in being able to actually use the measurements myself instead of just sending them all to The Weather Co for free.

    triq.org/rtl_433/

    #PWS

  11. Finally, this work would not have been possible without the input and work from all my co-authors from UK, France, Italy and USA. I am grateful that I could be part of this journee and want to thank also the #FoundationForPraderWilliResearch (#FPWR) for their generous funding! I hope that this research may at some day contribute to improve the life of patients with #PraderWilliSyndrome (#PWS) or other #RareDiseases.

    #TranslationalResearch #INFRAFRONTIER #IMPC

  12. Finally, this work would not have been possible without the input and work from all my co-authors from UK, France, Italy and USA. I am grateful that I could be part of this journee and want to thank also the #FoundationForPraderWilliResearch (#FPWR) for their generous funding! I hope that this research may at some day contribute to improve the life of patients with #PraderWilliSyndrome (#PWS) or other #RareDiseases.

    #TranslationalResearch #INFRAFRONTIER #IMPC

  13. Finally, this work would not have been possible without the input and work from all my co-authors from UK, France, Italy and USA. I am grateful that I could be part of this journee and want to thank also the #FoundationForPraderWilliResearch (#FPWR) for their generous funding! I hope that this research may at some day contribute to improve the life of patients with #PraderWilliSyndrome (#PWS) or other #RareDiseases.

    #TranslationalResearch #INFRAFRONTIER #IMPC

  14. Finally, this work would not have been possible without the input and work from all my co-authors from UK, France, Italy and USA. I am grateful that I could be part of this journee and want to thank also the #FoundationForPraderWilliResearch (#FPWR) for their generous funding! I hope that this research may at some day contribute to improve the life of patients with #PraderWilliSyndrome (#PWS) or other #RareDiseases.

    #TranslationalResearch #INFRAFRONTIER #IMPC

  15. Finally, this work would not have been possible without the input and work from all my co-authors from UK, France, Italy and USA. I am grateful that I could be part of this journee and want to thank also the #FoundationForPraderWilliResearch (#FPWR) for their generous funding! I hope that this research may at some day contribute to improve the life of patients with #PraderWilliSyndrome (#PWS) or other #RareDiseases.

    #TranslationalResearch #INFRAFRONTIER #IMPC

  16. Although the genetic cause of #PWS is known, therapeutic treatment primarly targets its symptoms. #PreclinicalResearch (often in mice) is essential to make progress on understanding the functioning of the involved genes and to develop new targeted therapies. In this research project we developed new PWS mouse models and analysed their phenotype (e.g., body features, behaviour and metabolism) using standardized experimental and analytical pipelines.

    #PraderWilliSyndrome #RareDisease

  17. Although the genetic cause of #PWS is known, therapeutic treatment primarly targets its symptoms. #PreclinicalResearch (often in mice) is essential to make progress on understanding the functioning of the involved genes and to develop new targeted therapies. In this research project we developed new PWS mouse models and analysed their phenotype (e.g., body features, behaviour and metabolism) using standardized experimental and analytical pipelines.

    #PraderWilliSyndrome #RareDisease

  18. Although the genetic cause of #PWS is known, therapeutic treatment primarly targets its symptoms. #PreclinicalResearch (often in mice) is essential to make progress on understanding the functioning of the involved genes and to develop new targeted therapies. In this research project we developed new PWS mouse models and analysed their phenotype (e.g., body features, behaviour and metabolism) using standardized experimental and analytical pipelines.

    #PraderWilliSyndrome #RareDisease

  19. Although the genetic cause of #PWS is known, therapeutic treatment primarly targets its symptoms. #PreclinicalResearch (often in mice) is essential to make progress on understanding the functioning of the involved genes and to develop new targeted therapies. In this research project we developed new PWS mouse models and analysed their phenotype (e.g., body features, behaviour and metabolism) using standardized experimental and analytical pipelines.

    #PraderWilliSyndrome #RareDisease

  20. Although the genetic cause of #PWS is known, therapeutic treatment primarly targets its symptoms. #PreclinicalResearch (often in mice) is essential to make progress on understanding the functioning of the involved genes and to develop new targeted therapies. In this research project we developed new PWS mouse models and analysed their phenotype (e.g., body features, behaviour and metabolism) using standardized experimental and analytical pipelines.

    #PraderWilliSyndrome #RareDisease

  21. #PWS is caused by a loss of function of genes on chromosome 15. These genes are peculiar, because they are in normal condition always expressed only from the paternal allele, the allele which is coming from the father, and not from both maternal and alleles – due to an epigenetic phenomenon called #GenomicImprinting. PWS patients either have parts of the paternal allele deleted or they have maternal uniparental disomy (#UPD) – a condition with effectively two maternal alleles instead of paternal and maternal alleles. This leads to a condition where some genes are not expressed at all, thus, their proteins and functions are missing for the proper development and functioning of the human body.

    #PraderWilliSyndrome #RareDisease

  22. #PWS is caused by a loss of function of genes on chromosome 15. These genes are peculiar, because they are in normal condition always expressed only from the paternal allele, the allele which is coming from the father, and not from both maternal and alleles – due to an epigenetic phenomenon called #GenomicImprinting. PWS patients either have parts of the paternal allele deleted or they have maternal uniparental disomy (#UPD) – a condition with effectively two maternal alleles instead of paternal and maternal alleles. This leads to a condition where some genes are not expressed at all, thus, their proteins and functions are missing for the proper development and functioning of the human body.

    #PraderWilliSyndrome #RareDisease

  23. #PWS is caused by a loss of function of genes on chromosome 15. These genes are peculiar, because they are in normal condition always expressed only from the paternal allele, the allele which is coming from the father, and not from both maternal and alleles – due to an epigenetic phenomenon called #GenomicImprinting. PWS patients either have parts of the paternal allele deleted or they have maternal uniparental disomy (#UPD) – a condition with effectively two maternal alleles instead of paternal and maternal alleles. This leads to a condition where some genes are not expressed at all, thus, their proteins and functions are missing for the proper development and functioning of the human body.

    #PraderWilliSyndrome #RareDisease

  24. #PWS is caused by a loss of function of genes on chromosome 15. These genes are peculiar, because they are in normal condition always expressed only from the paternal allele, the allele which is coming from the father, and not from both maternal and alleles – due to an epigenetic phenomenon called #GenomicImprinting. PWS patients either have parts of the paternal allele deleted or they have maternal uniparental disomy (#UPD) – a condition with effectively two maternal alleles instead of paternal and maternal alleles. This leads to a condition where some genes are not expressed at all, thus, their proteins and functions are missing for the proper development and functioning of the human body.

    #PraderWilliSyndrome #RareDisease

  25. #PWS is caused by a loss of function of genes on chromosome 15. These genes are peculiar, because they are in normal condition always expressed only from the paternal allele, the allele which is coming from the father, and not from both maternal and alleles – due to an epigenetic phenomenon called #GenomicImprinting. PWS patients either have parts of the paternal allele deleted or they have maternal uniparental disomy (#UPD) – a condition with effectively two maternal alleles instead of paternal and maternal alleles. This leads to a condition where some genes are not expressed at all, thus, their proteins and functions are missing for the proper development and functioning of the human body.

    #PraderWilliSyndrome #RareDisease

  26. Prader-Willi-Syndrome (PWS) is a rare genetic disorder, firstly described by Prader, Labhart and Willi in 1956 [1]. Individuals with PWS typically have feeding issues in early childhood, followed by obesity, but possible symptoms include social behavioural and intellectual problems:
    en.wikipedia.org/wiki/Prader%E

    [1] Prader, A., Labhart, A. & Willi, H. Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus
    und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter. Schweiz. Med.
    Wochenschr. 86, 1260–1261 (1956).

    #PraderWilliSyndrome #PWS #RareDisease

  27. Prader-Willi-Syndrome (PWS) is a rare genetic disorder, firstly described by Prader, Labhart and Willi in 1956 [1]. Individuals with PWS typically have feeding issues in early childhood, followed by obesity, but possible symptoms include social behavioural and intellectual problems:
    en.wikipedia.org/wiki/Prader%E

    [1] Prader, A., Labhart, A. & Willi, H. Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus
    und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter. Schweiz. Med.
    Wochenschr. 86, 1260–1261 (1956).

    #PraderWilliSyndrome #PWS #RareDisease

  28. Prader-Willi-Syndrome (PWS) is a rare genetic disorder, firstly described by Prader, Labhart and Willi in 1956 [1]. Individuals with PWS typically have feeding issues in early childhood, followed by obesity, but possible symptoms include social behavioural and intellectual problems:
    en.wikipedia.org/wiki/Prader%E

    [1] Prader, A., Labhart, A. & Willi, H. Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus
    und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter. Schweiz. Med.
    Wochenschr. 86, 1260–1261 (1956).

    #PraderWilliSyndrome #PWS #RareDisease

  29. Prader-Willi-Syndrome (PWS) is a rare genetic disorder, firstly described by Prader, Labhart and Willi in 1956 [1]. Individuals with PWS typically have feeding issues in early childhood, followed by obesity, but possible symptoms include social behavioural and intellectual problems:
    en.wikipedia.org/wiki/Prader%E

    [1] Prader, A., Labhart, A. & Willi, H. Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus
    und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter. Schweiz. Med.
    Wochenschr. 86, 1260–1261 (1956).

    #PraderWilliSyndrome #PWS #RareDisease

  30. Prader-Willi-Syndrome (PWS) is a rare genetic disorder, firstly described by Prader, Labhart and Willi in 1956 [1]. Individuals with PWS typically have feeding issues in early childhood, followed by obesity, but possible symptoms include social behavioural and intellectual problems:
    en.wikipedia.org/wiki/Prader%E

    [1] Prader, A., Labhart, A. & Willi, H. Ein Syndrom von Adipositas, Kleinwuchs, Kryptorchismus
    und Oligophrenie nach myatonieartigem Zustand im Neugeborenenalter. Schweiz. Med.
    Wochenschr. 86, 1260–1261 (1956).

    #PraderWilliSyndrome #PWS #RareDisease

  31. Today, I am happy to share with you our recent manuscript, “The Preclinical Animal Network (PCAN): Integrative high-throughput phenotyping of standardized mouse models for Prader-Willi syndrome”, available on @biorxivpreprint
    biorxiv.org/content/10.1101/20

    #PraderWilliSyndrome #PWS #GenomicImprinting #RareDisease #DigitalTwin #MouseGenetics #FPWR

  32. Today, I am happy to share with you our recent manuscript, “The Preclinical Animal Network (PCAN): Integrative high-throughput phenotyping of standardized mouse models for Prader-Willi syndrome”, available on @biorxivpreprint
    biorxiv.org/content/10.1101/20

    #PraderWilliSyndrome #PWS #GenomicImprinting #RareDisease #DigitalTwin #MouseGenetics #FPWR

  33. Today, I am happy to share with you our recent manuscript, “The Preclinical Animal Network (PCAN): Integrative high-throughput phenotyping of standardized mouse models for Prader-Willi syndrome”, available on @biorxivpreprint
    biorxiv.org/content/10.1101/20

    #PraderWilliSyndrome #PWS #GenomicImprinting #RareDisease #DigitalTwin #MouseGenetics #FPWR

  34. Today, I am happy to share with you our recent manuscript, “The Preclinical Animal Network (PCAN): Integrative high-throughput phenotyping of standardized mouse models for Prader-Willi syndrome”, available on @biorxivpreprint
    biorxiv.org/content/10.1101/20

    #PraderWilliSyndrome #PWS #GenomicImprinting #RareDisease #DigitalTwin #MouseGenetics #FPWR

  35. Today, I am happy to share with you our recent manuscript, “The Preclinical Animal Network (PCAN): Integrative high-throughput phenotyping of standardized mouse models for Prader-Willi syndrome”, available on @biorxivpreprint
    biorxiv.org/content/10.1101/20

    #PraderWilliSyndrome #PWS #GenomicImprinting #RareDisease #DigitalTwin #MouseGenetics #FPWR