chip | Tail multiple remote | Command Line Interface library

Google Docs has recently introduced a feature where we can refer to

• Date
• Person
• Google Drive Document

in the form of a Chip Block (as shown in the picture above)

I am trying to generate such chip block using Google App Script.

Rich Link Documentation does not have any code snippet or method to add a Rich Link inside a document.

Document Service page also doesn't have detail regarding how to insert a Rich Link.

I wonder whether the feature is not yet implemented in the Google App Script Api

i have been trying to follow these guide to learn NX, but i encounter this problem when i tried to serve the nestJs api you can see the complete code on this repo

Hi am facing an issue while running flutter project in MacBook Air M1 chip Lap. Tried all possibilities couldn't find where is the exact problem.

All basic solutions like flutter clean, flutter pub get, pod deintegrate & install, flutter build ios, flutter run but still same issue. only on iOS simulator not deploying.

Any solution for this. Thanks in advance.

Error

In my XML I'm just declaring a ChipGroup as follows:

My new Macbook Pro running on an M1 Max (ARM) chip just came in. I installed Parallels and Windows 11 Preview for ARM, and Visual Studio installs / launches / builds my solution beautifully. Unfortunately the turn windows features on or off dialog doesn't have the option for installing IIS, and others have posted that this is not supported in Windows 11 for ARM.

Our dev team runs multiple ASP.NET Core 3.1 websites locally under IIS using subdomains, e.g.: https://auth-dev.mydomain.com, https://web-dev.mydomain.com, https://webapi-dev.mydomain.com. This was easy to set up in IIS using the bindings dialog, I could specify for port 443 (https) to use a certain subdomain and our dev SSL certificate.

Now I need to figure out how to make this work on Windows 11 ARM. Developing on an inferior non-Macbook Pro laptop doesn't seem like a great solution for .NET devs, I have to assume others with M1 chip Macbook Pros have run into this same issue. What are my options?

I first started looking into using IIS Express, but it seems like every website has to run on a different port, whereas I need them all to run on port 80 (just with different subdomains.) I'd be fine with them running on different ports if there was a way to forward those various ports to the subdomains, but it doesn't seem like the windows HOSTS file supports that.

I also looked into using the Apache web server for Windows, but I read somewhere that it doesn't support running ASP.NET Core apps.

I have Android Studio BumbleBee 2021.1.1 downloaded, running on a MacBook Pro M1. When downloading Android Studio, I chose the Apple Chip option (opposed to Intel)

I've created a Virtual Device - Android 12.0 arm64-v8a Pixel 4.

When I attempt to run the emulator it gets stuck here

Then, it times out:

I have searched SO and other blogs and can only find outdated material based on a time in 2020/2021 when Android did not support ARM64. However, it's my understanding that this has now changed so https://github.com/google/android-emulator-m1-preview is no longer needed.

What is the correct way to run the Android Emulator on a Mac with an M1 Chip?

I would like to implement forward-chaining reasoning in Prolog. I made up a simple KB of facts and some rules, from which I should be able to get the fact green(fritz). I tried to implement it but somehow, when member fails, it stops going on.

I've downloaded Android Studio from the official website, the one for M1 chip (arm).

Basically running it for the first time, the error is the following:

Unambiguous DNA sequences consist only of the nucleobases adenine (A), cytosine (C), guanine (G), thymine (T). For human consumption, the bases may be represented by the corresponding char in either uppercase or lowercase: A, C, G, T, or a, c, g, t. This representation is inefficient, however, when long sequences need to be stored. Since only four symbols need to be stored, each symbol can be assigned a 2-bit code. The commonly used .2bit-format specified by UCSC does exactly that, using the following encoding: T = 0b00, C = 0b01, A = 0b10, G = 0b11.

The C code below shows a reference implementation written for clarity. Various open-source software that converts genomic sequences represented as a char sequence typically uses a 256-entry lookup table indexed by each char in sequence. This also isolates from the internal representation of char. However, memory access is energetically expensive, even if the access is to an on-chip cache, and generic table look-ups are difficult to SIMDize. It would therefore be advantageous if the conversion could be accomplished by simple integer arithmetic. Given that ASCII is the dominating char encoding, one can restrict to that.

What are efficient computational approaches to convert nucleobases given as ASCII characters to their .2bit-representation?