Chris W Whelan

The current admissions system based on SES zones and bonus points excludes many kids with A grades and high test scores, especially those from Catholic schools like yours. If we are going to stick with that system then increasing the number of seats seems like the right thing to do to me.

If this happens, this policy change will prevent discoveries and will result in our children and grandchildren being sicker and dying sooner

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2/n

If doing CNV calling the default bin size in GATK gCNV for Illumina data is 1kb. I’d look at the histogram and MAD of 1kb bin depths. If its not tight or your regions of interest contain lots of repetitive sequence 5 or 10kb might work (with less resolution)

Not window size based, but we often use metrics like “Percent bases at 20X coverage” to QC WGS data for variant calling.

I'm sort of skeptical that that's the case at selective schools, which in my experience liked well-rounded applicants, but maybe things have changed.

Genuine question -- why not just push for rigorous college-prep level high school humanities classes then? I confess I do not get the appeal of Early College as currently presented. Seems like quasi-vocational "career-track" stuff instead of a chance to actually explore college-level classes early.

What Wu policies are responsible for the low homicide rate?

Today is the FINAL day to submit your bids in our Silent Auction for a Healthy Ocean!

Bidding closes at 8 PM Eastern! Jenna and Sarah will be going LIVE on Instagram at 4 PM to showcase some of the incredible auction items—tune in to catch the action! ow.ly/5vVf50UkggC

I put some #rstats code into Claude and told it to optimize it. It totally rewrote it and got a 50x speed up with identical results. …maybe we actually are cooked?

Lifelong JP resident. BPS grad and (unhappy) BPS parent.

As part of #gnomAD v4, in collaboration with the Talkowski Lab, we have released 1,199,117 genome SVs and 66,903 rare exome CNVs. These data represent the first gnomAD SV dataset released native to the GRCh38 reference genome. (1/2)

The #gnomAD team is proud to announce the release of gnomAD v4! The v4 dataset includes 730,947 exomes & 76,215 genomes, which is ~5x larger than the v2 & v3 releases combined, & includes nearly 120K indivs of non-European genetic ancestry broad.io/gnomad #ASHG23 (1/11)