(BY MR. BLASIER) Mr. Sims, as we said a few minutes ago, the hints and traces of dots that I had on my board that we just talked about, those were taken from your laboratory's results, correct?
I believe they were, except there was that one use of the word "vary." I don't think that was from my actual worksheet.
Well, that's one of their boards. I was talking about the Bronco board.
The testing strips that were on it had traces and hints?
Yes, I think by and large, that was the language.
I didn't look at each one against my recent sheets, but that sounds familiar.
You would agree, would you not, that the problems of interpretation of these things become more complicated when you're dealing with very small quantities of DNA and faint dots like this?
And sometimes it's not unusual to look at a picture and not see any dots at all, and then look at it in a little different light, and all of a sudden, you see a hint of something, correct?
Well we -- in our laboratory, we really struggle with dots. We really look at them in such a way that we don't want to overlook anything. We call it very close.
We look to see if there's anything at all there, we'll call it. We're very -- what's the word -- persnickety about that.
I don't know if there's another right word.
KEY QUOTEIs -- one of the reasons for that is the only thing that can light up any of those dots is DNA?
The only thing would be DNA, unless there's something totally wrong with the dot; that's correct, yes.
Okay.
So if you see a hint, a trace, a smudge or little tiny dot, you know that there is DNA on there; it may be from contamination, may be cross-hybridization, may be a DX gene, but you know it's DNA?
Stain number 303 was a stain that was taken from the console area on August 24. You're aware of that, are you not?
And stain number 30 is a stain taken from the same area or similar area on June 14, correct?
Thank you.
Now, I want to talk about the Bundy drops for a minute.
The swatches that were sent to you from LAPD for the Bundy drops were in bindles, correct? In envelopes?
Now, one of those bindles for Bundy drop number 47, you made note that there was a transfer -- a wet transfer of a blood stain on the bindle itself. Do you recall that?
And that's consistent which a swatch being put in that bindle while it's still wet, is it not?
Yes.
In other words, there would be some dampness to it that would transfer the blood to the bindle material.
And I want to close by asking you some questions about the socks.
When you got the socks, you could see several stains with your naked eye, could you not?
Well, when I got the socks, I saw, for example, cut-out areas and circled areas, so I knew to look at those areas first.
I could see them with the naked eye to some extent where I -- when I knew where to look, yes.
Now, you testified on direct, I believe, that you saw part of the ankle stain of the -- one of the socks had a big cut-out on it.
You were actually sent some of the patches that had been cut out of that center area, correct?
There's the large sample that RFLP results indicated 11 probes, I think, Nicole Brown Simpson?
And you also observed, if we look at a sock and consider a sock as having four surfaces on it, the outside, the inside, and the inside of the other side, and the outside?
You saw blood on the opposite side of the sock on surface three that corresponded to that cut-out area, did you not?
Well, I don't think that really characterizes what I saw.
In fact, when I did that examination, what I noted in my notes is that it did not appear that there was any transfer to that third surface. There were some fibrils with blood on them that had flaked off; and it had appeared to me, once you start cutting this sock material the, fibrils can come -- they start to ravel, basically.
And you did what's called a yield gel, which helps you determine how much DNA is on those stains; and you did that process on three of those swatches, correct?
And on those three swatches, which aren't even the entire stain, you found an estimated 1315 nanograms of DNA, correct?
Yes, I took three of the four pieces and I -- after I ran my yield gel, I had about 1350 nanograms left.
KEY QUOTEAnd of all of the stains, I think you said there was 108, or over 100 that you processed in this case, that was by far the largest amount of DNA in any stain, correct, other than the reference samples?
In our laboratory, we really struggle with dots. We really look at them in such a way that we don't want to overlook anything. We call it very close. We look to see if there's anything at all there, we'll call it. We're very -- what's the word -- persnickety about that.
I don't recall seeing AM on any of those Bundy bindles.
Yes, I took three of the four pieces and I -- after I ran my yield gel, I had about 1350 nanograms left.
You didn't put any EDTA on those swatches, did you?